ChemWiki - User contributions [en]

Rep:Mod:im3117

2019-05-20T15:26:06Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -12.3847 -12.3783 -5.6131 -0.0040 0.0194 0.0711
Low frequencies --- 100.9307 100.9314 147.2333
</pre>

Frequency file: [[Media:IM_NI3_Freq_2.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 [Date Accessed: 16 May 2019] </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2. Available from: http://www.wiredchemist.com/chemistry/data/bond_energies_lengths.html [Date Accessed: 19 May 2019] </ref>
</references>

Rep:Mod:im3117

2019-05-20T15:25:25Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM_NI3_Freq_2.log| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 [Date Accessed: 16 May 2019] </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2. Available from: http://www.wiredchemist.com/chemistry/data/bond_energies_lengths.html [Date Accessed: 19 May 2019] </ref>
</references>

File:IM NI3 Freq 2.LOG

2019-05-20T15:24:32Z

Im3117:

Rep:Mod:im3117

2019-05-19T13:54:13Z

Im3117: /* NH3BH3 */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 [Date Accessed: 16 May 2019] </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2. Available from: http://www.wiredchemist.com/chemistry/data/bond_energies_lengths.html [Date Accessed: 19 May 2019] </ref>
</references>

Rep:Mod:im3117

2019-05-19T13:53:52Z

Im3117: /* NH3 */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 [Date Accessed: 16 May 2019] </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2. Available from: http://www.wiredchemist.com/chemistry/data/bond_energies_lengths.html [Date Accessed: 19 May 2019] </ref>
</references>

Rep:Mod:im3117

2019-05-19T13:53:26Z

Im3117: /* References */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 [Date Accessed: 16 May 2019] </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2. Available from: http://www.wiredchemist.com/chemistry/data/bond_energies_lengths.html [Date Accessed: 19 May 2019] </ref>
</references>

Rep:Mod:im3117

2019-05-19T13:50:50Z

Im3117: /* Energies */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />. Compared with a N-N bond, whose bond strength is 167 kJmol-1, the bond is weaker. The decreased bond strength can be attributed to the dative nature of the bond as the electrons both come from the nitrogen lone pair and are donated into the boron's empty p orbital.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2.</ref>
</references>

Rep:Mod:im3117

2019-05-19T13:44:31Z

Im3117: /* Energies */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker<ref name="Cottrell" />.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2.</ref>
</references>

Rep:Mod:im3117

2019-05-19T13:43:54Z

Im3117: /* References */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
<ref name="Cottrell">Cottrell T L. The Strengths of Chemical Bonds. 1958. 2.</ref>
</references>

Rep:Mod:im3117

2019-05-17T19:48:07Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 21'''

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:47:46Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''

'''Settings''': B3LYP/6-31G(d,p)

<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:46:01Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above. Nitrogen is more electronegative than phosphorus as it has a smaller atomic radius so the effective nuclear charge felt by the electrons is increased. There is also less shielding by inner electrons for nitrogen as it has fewer shells of electrons.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:41:55Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19<ref name="Pauling" />. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:41:24Z

Im3117: /* Energies */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated<ref name="Pauling" />. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:40:15Z

Im3117: /* References */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

=References=
<references>
<ref name="Pauling">Pauling L. The Nature of the Chemical Bond. IV. The Energy of Single Bonds and the Relative Electronegativity of Atoms. Journal of the American Chemical Society. 1932:54(9):3570-3582. doi: 10.1021/ja01348a011 </ref>
</references>

Rep:Mod:im3117

2019-05-17T19:32:11Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the more negatively charged the atom, i.e. the more electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

=References=
<references>

Rep:Mod:im3117

2019-05-17T19:31:24Z

Im3117:

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

=References=
<references>

Rep:Mod:im3117

2019-05-17T19:30:37Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:Mo18analysis.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T19:30:13Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[Mo18analysis.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

File:Mo18analysis.PNG

2019-05-17T19:29:59Z

Im3117:

Rep:Mod:im3117

2019-05-17T19:26:33Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Optimisation file: [[Media:NI3_VERS2_IM.LOG| NI3_Optimisation.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:33:38Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

'''Figure 4'''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:31:42Z

Im3117: /* Real MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure 3, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:31:24Z

Im3117: /* Real MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

There are no significant differences between the real and LCAO MOs. The LCAO MOs allow the prediction of the number of nodes and therefore the bonding or antibonding character of the orbital. The shape of the orbitals is somewhat harder to predict however they do fall in line with the LCAO predictions in terms of phases. Qualitative MO theory is very useful and accurate however some flaws can exist when interpreting the energetic ordering of some of the frontier molecular orbitals. This is because it can be hard to quantify the interactions between orbitals and which effect has greater importance in a specific instance. For example, in the MO diagram, as seen in Figure X, the prediction of the ordering of 3a1' versus 2e' was hard to quantify.

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:25:28Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 9.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:23:03Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

The lower the value in the table above, the higher the electron density around it. The nitrogen is has a more negative charge than the phosphorus as it is more electronegative so has more electron density around it. Nitrogen has a high Pauling electronegativity of 3.04, whereas phosphorus is 2.19. As a result of its lone pair being tightly held, less electron density is donated to form the dative bond with carbon so the carbon has less electron density around it, as reflected in the table above.

Rep:Mod:im3117

2019-05-17T13:13:33Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character, higher in energy as there are more nodes than in the molecular orbital above however there still aren't many nodes || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding character, higher in energy again as there are multiple nodes || Y || [[File:MO_Analysis_18_IM.PNG|400px]]
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T12:59:18Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y || [[File:Analysis10_IM.PNG|400px]]
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

File:Analysis10 IM.PNG

2019-05-17T12:58:45Z

Im3117:

Rep:Mod:im3117

2019-05-17T12:55:54Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character, 1 node || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T12:55:28Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character || Y || [[File:Analysis7_IM.PNG|400px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T12:55:09Z

Im3117: /* MO Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character || Y || [[File:Analysis7_IM.PNG|350px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T12:54:51Z

Im3117: /* MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

=== MO Analysis ===

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character || Y || [[File:Analysis7_IM.PNG|200px]]
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

File:Analysis7 IM.PNG

2019-05-17T12:54:09Z

Im3117:

Rep:Mod:im3117

2019-05-17T12:43:01Z

Im3117: /* MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 7 || -0.93 || [[File:CHOSENMO_7.PNG|200px]] || Bonding character || Y
|-
| 10 || -0.81 || [[File:CHOSENMO_10.PNG|200px]] || Bonding character || Y
|-
| 18 || -0.58 || [[File:CHOSENMO_18.PNG|200px]] || More antibonding chara|| Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

File:CHOSENMO 18.PNG

2019-05-17T12:39:06Z

Im3117:

File:CHOSENMO 10.PNG

2019-05-17T12:38:48Z

Im3117:

File:CHOSENMO 7.PNG

2019-05-17T12:38:30Z

Im3117:

Rep:Mod:im3117

2019-05-17T12:21:38Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.12</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T12:21:00Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:NI3_VERS2_IM.LOG| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>NI3_VERS2_IM.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

File:NI3 VERS2 IM.LOG

2019-05-17T12:20:14Z

Im3117:

Rep:Mod:im3117

2019-05-17T12:07:10Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Table_IM_NI3.PNG|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

File:Table IM NI3.PNG

2019-05-17T12:06:54Z

Im3117:

Rep:Mod:im3117

2019-05-17T12:06:27Z

Im3117: /* Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000067 0.000450 YES
RMS Force 0.000044 0.000300 YES
Maximum Displacement 0.000492 0.001800 YES
RMS Displacement 0.000333 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:45:15Z

Im3117: /* MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:44:40Z

Im3117: /* MOs */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -14.6 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -10.4 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -10.4 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -10.4 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -10.4 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || -1.20 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || -0.93 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || -0.93 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || -0.93 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || -0.81 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || -0.70 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || -0.70 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || -0.70 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || -0.62 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || -0.62 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || -0.580 || [[File:MO_IM_16.PNG|200px]] || Valence || Y
|-
| 17 || -0.580 || [[File:MO_IM_17.PNG|200px]] || Valence || Y
|-
| 18 || -0.580 || [[File:MO_IM_18.PNG|200px]] || Valence || Y
|-
| 19 || -0.579 || [[File:MO_IM_19.PNG|200px]] || Valence || Y
|-
| 20 || -0.579 || [[File:MO_IM_20.PNG|200px]] || Valence || Y
|-
| 21 || -0.579 || [[File:MO_IM_21.PNG|200px]] || Valence || Y
|-
| 22 || -0.13 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || -0.069 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || -0.067 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || -0.067 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || -0.067 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

Note: for MOs 16-21 and 23-26, more significant figures were given to provide distinction between non-degenerate levels.

{| class="wikitable"
|+ Table 19
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled? || Theory Prediction
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:32:30Z

Im3117: /* Comparisons */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -0.35 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -0.07 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || 0.17 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || 0.18 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || 0.18 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || 0.18 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || 0.18 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || 0.18 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || 0.18 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || 0.18 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || 0.18 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || 0.18 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || 0.18 || [[File:MO_IM_16.PNG|200px]] || Valence || N
|-
| 17 || 0.18 || [[File:MO_IM_17.PNG|200px]] || Valence || N
|-
| 18 || 0.18 || [[File:MO_IM_18.PNG|200px]] || Valence || N
|-
| 19 || 0.18 || [[File:MO_IM_19.PNG|200px]] || Valence || N
|-
| 20 || 0.18 || [[File:MO_IM_20.PNG|200px]] || Valence || N
|-
| 21 || 0.18 || [[File:MO_IM_21.PNG|200px]] || Valence || N
|-
| 22 || 0.18 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || 0.18 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || 0.18 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || 0.18 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || 0.18 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 25
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 9'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 26
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:32:08Z

Im3117: /* Charge Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -0.35 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -0.07 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || 0.17 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || 0.18 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || 0.18 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || 0.18 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || 0.18 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || 0.18 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || 0.18 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || 0.18 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || 0.18 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || 0.18 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || 0.18 || [[File:MO_IM_16.PNG|200px]] || Valence || N
|-
| 17 || 0.18 || [[File:MO_IM_17.PNG|200px]] || Valence || N
|-
| 18 || 0.18 || [[File:MO_IM_18.PNG|200px]] || Valence || N
|-
| 19 || 0.18 || [[File:MO_IM_19.PNG|200px]] || Valence || N
|-
| 20 || 0.18 || [[File:MO_IM_20.PNG|200px]] || Valence || N
|-
| 21 || 0.18 || [[File:MO_IM_21.PNG|200px]] || Valence || N
|-
| 22 || 0.18 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || 0.18 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || 0.18 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || 0.18 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || 0.18 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 24
|-
| Atom (in [P(CH3)4]+) || Charge (C)
|-
| P || 1.666
|-
| C || -1.060
|-
| H || 0.298
|}

== Comparisons ==

{| class="wikitable"
|+ Table 24
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 8'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 25
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:31:04Z

Im3117: /* Charge Analysis */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -0.35 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -0.07 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || 0.17 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || 0.18 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || 0.18 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || 0.18 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || 0.18 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || 0.18 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || 0.18 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || 0.18 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || 0.18 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || 0.18 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || 0.18 || [[File:MO_IM_16.PNG|200px]] || Valence || N
|-
| 17 || 0.18 || [[File:MO_IM_17.PNG|200px]] || Valence || N
|-
| 18 || 0.18 || [[File:MO_IM_18.PNG|200px]] || Valence || N
|-
| 19 || 0.18 || [[File:MO_IM_19.PNG|200px]] || Valence || N
|-
| 20 || 0.18 || [[File:MO_IM_20.PNG|200px]] || Valence || N
|-
| 21 || 0.18 || [[File:MO_IM_21.PNG|200px]] || Valence || N
|-
| 22 || 0.18 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || 0.18 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || 0.18 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || 0.18 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || 0.18 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 8'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

== Comparisons ==

{| class="wikitable"
|+ Table 24
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 8'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 25
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}

Rep:Mod:im3117

2019-05-17T11:30:27Z

Im3117: /* Charge Density */

= im3117 Inorganic Wiki Page =

== BH3 Molecule ==

=== Analysis ===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 1'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000193 0.000450 YES
RMS Force 0.000126 0.000300 YES
Maximum Displacement 0.000764 0.001800 YES
RMS Displacement 0.000500 0.001200 YES
</pre>

'''Table 2'''
<pre>
Low frequencies --- -0.2261 -0.1036 -0.0054 48.0227 49.0824 49.0830
Low frequencies --- 1163.7223 1213.6713 1213.6740
</pre>

Frequency file: [[Media:IM_BH3_FREQ.LOG| BH3_Frequency.log]]

'''Figure 1'''
<jmol><jmolApplet>
<title>optimised BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_BH3_SYM_OPT_2.LOG</uploadedFileContents>
<script>frame 1.4</script>
</jmolApplet></jmol>

Lowest frequency is outside the suggested ± 15 cm-1 range. This can be the case for small molecules as the frequencies can be attributed to the basicity of the basis set and the relatively relaxed convergence and integration criteria.

===Vibrational spectrum for BH3===

{| class="wikitable"
|+ Table 3
|-
|wavenumber (cm-1) || Intensity (arbitrary units) || symmetry || IR active? || type
|-
|1164
|92
|A''2
|yes
|out-of-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|1214
|14
|E'
|very slight
|in-plane bend
|-
|2580
|0
|A'1
|no
|totally symmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|-
|2713
|126
|E'
|yes
|asymmetric stretch
|}

'''Figure 2'''

[[File:Bh3_spectrum_1.png|300px]]

There are fewer vibrational peaks than vibrations as not all of the vibrations are IR active. To satisfy the selection rules for IR activity, a bend/stretch must result in a change in dipole moment. As the symmetric stretch (2580 cm-1) does not have a change in dipole moment, it is not visible on the spectrum.

===PP and Basis Sets===

'''Table 4'''

[[File:Bh3 summary table 1.png|300px]]

''A table produced by Gaussian indicating the features of the optimised BH3 molecule.''

=== MO Diagram ===

'''Figure 3'''

[[File:IM_Full_MO.png|500px]]

A qualitative MO diagram indicating the predicted ordering of the BH3 orbitals. The 1a1 ' is too low in energy to interact with the a1' symmetry atomic orbitals from the H3 fragment. It therefore solely comprises boron atomic orbitals. 2a1' has larger contribution from H3 as the molecular orbital is closer in energy to its atomic orbitals. The 1e' orbitals are low in energy due to the in-phase overlap between the atomic orbitals, producing a frontier orbital with a larger contribution from H3 due to it being closer in energy. 1a2'' ''is a non-bonding orbital as there are no other atomic orbitals with the same symmetry for it to interact with. As there is no interaction, the orbitals is neither raised nor lowered in energy. The 3a1' orbital has a larger contribution from the boron 2s orbital as it is closer in energy to this frontier orbital. It is more destabilised than the 2a1' is stabilised. The 2e' orbitals are anti-bonding molecular orbitals as they contain out-of-phase overlap with greater contribution from boron's 2p orbitals as they are higher in energy and therefore closer in energy. The relative ordering of 3a1 ' and 2e' is difficult to ascertain as s-s interactions are stronger, however a1' are lower than e'.

=== Real MOs ===

{| class="wikitable"
|+ Table 5
|-
| MO (incl. symmetry) || Energy (eV)|| Picture || Theory Prediction ||Filled?
|-
| 1a1' || -6.77 || [[File:IM_BH3_1.PNG|200px]] || [[File:IM_BH3_T_1.png|200px]] || Y
|-
| 2a1' || -0.51 || [[File:IM_BH3_2.PNG|200px]] || [[File:IM_BH3_T_2.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_3.PNG|200px]] || [[File:IM_BH3_T_3.png|200px]] || Y
|-
| 1e' || -0.35 || [[File:IM_BH3_4.PNG|200px]] || [[File:IM_BH3_T_4.png|200px]] || Y
|-
| 1a2'' || -0.07 || [[File:IM_BH3_5.PNG|200px]] || [[File:IM_BH3_T_5.png|200px]] || N
|-
| 3a1' || 0.17 || [[File:IM_BH3_6.PNG|200px]] || [[File:IM_BH3_T_6.png|200px]] || N
|-
| 2e' || 0.18 || [[File:IM_BH3_7.PNG|200px]] || [[File:IM_BH3_T_7.png|200px]] || N
|}

Are there any significant differences between the real and LCAO MOs? What does this say about the accuracy and usefulness of qualitative MO theory?

== NH3 ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

NH3 optimised bond length = 1.02 Å ; H-N-H optimised bond angle = 105.7 °

'''Table 6'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000006 0.000450 YES
RMS Force 0.000004 0.000300 YES
Maximum Displacement 0.000012 0.001800 YES
RMS Displacement 0.000008 0.001200 YES

</pre>

'''Table 7'''

<pre>
Low frequencies --- -8.5646 -8.5588 -0.0044 0.0454 0.1784 26.4183
Low frequencies --- 1089.7603 1694.1865 1694.1865
</pre>

Frequency file: [[Media:IM_NH3_FREQ2.LOG | NH3_Frequency.log]]

'''Table 8'''

[[File:NH3_Table.PNG|300px]]

''A table produced by Gaussian indicating the features of the optimised NH3 molecule.''

<jmol><jmolApplet>
<title>optimised NH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3_FREQ2.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

== NH3BH3 ==

===Analysis===
'''Settings''': B3LYP/6-31G(d,p)

Optimised bond lengths: B-N = 1.67 Å; B-H = 1.21 Å; N-H = 1.02 Å

Optimised bond angles: H-B-H = 113.9 °; H-N-H = 107.9 °

'''Table 9'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000233 0.000450 YES
RMS Force 0.000083 0.000300 YES
Maximum Displacement 0.001202 0.001800 YES
RMS Displacement 0.000370 0.001200 YES
</pre>

'''Table 10'''

<pre>
Low frequencies --- -0.0277 -0.0069 -0.0053 10.0759 10.1235 37.9189
Low frequencies --- 265.3049 634.4304 639.2081
</pre>

Frequency file: [[Media: IM_NH3BH3_OPTFREQ2.LOG | NH3BH3_Frequencies.log]]

'''Table 11'''

[[File:IM_TABLE_VERS2.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NH3BH3_OPTFREQ2.LOG</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

=== Energies ===

1 a.u. = 627.5 kcal/mol
1 a.u. = 2625 kJ/mol

E(NH3)= -56.55777 au (to 5 dp)

E(BH3)= -26.61532 au (to 5 dp)

E(NH3BH3)= -83.22469 (to 5 dp)

ΔE = E(NH3BH3)-[E(NH3)+E(BH3)]
= -83.22469 - [-56.55777-26.61532]
= 0.0516 au
= 135 kJmol-1 (to nwn)

Based on my energy calculation is the B-N dative bond weak, medium or strong? By comparing the electronegativities of B and N, 2.04 and 3.04 respectively, the B-N bond is a polar covalent bond but the charge density is not incredibly separated. The elements also occupy the same period of the periodic table meaning there is increased overlap between the orbitals, strengthening the bond. The lone pair on the NH3 also quenches the Lewis acidity of the BH3, arising due to the electron deficiency in the empty p orbital. All of these factors suggest that the B-N is a medium strength bond. However in comparison with the isoelectronic C-C bond, 346 kJmol-1, it is weaker.

== NI3 Molecule ==

===Analysis===

'''Settings''': B3LYP/6-31G(d,p)LANL2DZ

Optimised N-I bond distance = 2.18 Å

'''Table 12'''

[[File:Ni3 opt table.png|300px]]

'''Table 13'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000061 0.000450 YES
RMS Force 0.000037 0.000300 YES
Maximum Displacement 0.000731 0.001800 YES
RMS Displacement 0.000357 0.001200 YES
</pre>

'''Table 14'''
<pre>
Low frequencies --- -5.5593 -5.4903 -0.0003 -0.0002 -0.0002 6.5127
Low frequencies --- 101.1566 101.2827 148.4563
</pre>

Frequency file: [[Media:IM NI3 OPT 1 2.gjf| NI3_Frequency.log]]

'''Figure 4'''
<jmol><jmolApplet>
<title> optimised NI3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>Ni3_opt_1_im.txt</uploadedFileContents>
<script>frame 1.16</script>
</jmolApplet></jmol>

== [N(CH3)4]+ ==
===Analysis===

'''Settings''': B3LYP/6-31G(d,p)

'''Table 15'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000073 0.000450 YES
RMS Force 0.000018 0.000300 YES
Maximum Displacement 0.000277 0.001800 YES
RMS Displacement 0.000088 0.001200 YES
</pre>

'''Table 16'''
<pre>
Low frequencies --- 0.0008 0.0009 0.0011 35.6259 35.6259 35.6259
Low frequencies --- 215.5175 315.1186 315.1186
</pre>

Frequency file: [[Media:IM_NCH34_SYMMFREQ1.LOG | N(CH3)4+_Frequency.log]]

These zero frequencies are higher than anticipated however is sufficient for this purpose. These values occur because the basis set used is insufficient to detect some of the more subtle vibrational modes.

'''Table 17'''

[[File:IM_N(CH3)4.PNG|300px]]

'''Figure 5'''

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_NCH34_SYMMFREQ1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===MOs===

{| class="wikitable"
|+ Table 18
|-
| MO Number || Energy (eV)|| Picture || Notes || Filled?
|-
| 1 || -6.77 || [[File:MO_IM_1.PNG|200px]] || Core || Y
|-
| 2 || -0.51 || [[File:MO_IM_2.PNG|200px]] || Core || Y
|-
| 3 || -0.35 || [[File:MO_IM_3.PNG|200px]] || Core || Y
|-
| 4 || -0.35 || [[File:MO_IM_4.PNG|200px]] || Core || Y
|-
| 5 || -0.07 || [[File:MO_IM_5.PNG|200px]] || Core || Y
|-
| 6 || 0.17 || [[File:MO_IM_6.PNG|200px]] || Valence || Y
|-
| 7 || 0.18 || [[File:MO_IM_7.PNG|200px]] || Valence || Y
|-
| 8 || 0.18 || [[File:MO_IM_8.PNG|200px]] || Valence || Y
|-
| 9 || 0.18 || [[File:MO_IM_9.PNG|200px]] || Valence || Y
|-
| 10 || 0.18 || [[File:MO_IM_10.PNG|200px]] || Valence || Y
|-
| 11 || 0.18 || [[File:MO_IM_11.PNG|200px]] || Valence || Y
|-
| 12 || 0.18 || [[File:MO_IM_12.PNG|200px]] || Valence || Y
|-
| 13 || 0.18 || [[File:MO_IM_13.PNG|200px]] || Valence || Y
|-
| 14 || 0.18 || [[File:MO_IM_14.PNG|200px]] || Valence || Y
|-
| 15 || 0.18 || [[File:MO_IM_15.PNG|200px]] || Valence || Y
|-
| 16 || 0.18 || [[File:MO_IM_16.PNG|200px]] || Valence || N
|-
| 17 || 0.18 || [[File:MO_IM_17.PNG|200px]] || Valence || N
|-
| 18 || 0.18 || [[File:MO_IM_18.PNG|200px]] || Valence || N
|-
| 19 || 0.18 || [[File:MO_IM_19.PNG|200px]] || Valence || N
|-
| 20 || 0.18 || [[File:MO_IM_20.PNG|200px]] || Valence || N
|-
| 21 || 0.18 || [[File:MO_IM_21.PNG|200px]] || Valence || N
|-
| 22 || 0.18 || [[File:MO_IM_22.PNG|200px]] || Valence || N
|-
| 23 || 0.18 || [[File:MO_IM_23.PNG|200px]] || Valence || N
|-
| 24 || 0.18 || [[File:MO_IM_24.PNG|200px]] || Valence || N
|-
| 25 || 0.18 || [[File:MO_IM_25.PNG|200px]] || Valence || N
|-
| 26 || 0.18 || [[File:MO_IM_26.PNG|200px]] || Valence || N
|}

===Charge Density===

'''Figure 6'''

[[File:IM_N(CH3)4_Charges.PNG|300px]]

{| class="wikitable"
|+ Table 20
|-
| Atom (in [N(CH3)4]+) || Charge (C)
|-
| N || -0.295
|-
| C || -0.483
|-
| H || 0.269
|}

[[File:IM_NR4_CHARGE.PNG|150px|thumb|right| Figure 7]]

Typically, NR4+ is portrayed as seen in Figure 7, which is supported by the charge distribution analysis seen in the table above, Table 20. This positive charge is a Lewis charge, arising from the fact that the nitrogen uses its Lewis basic lone pair of electrons and donates them to form a bond with an alkyl group. It also arises from the fact that nitrogen only has 3 unpaired electrons and therefore would expect to form only three bonds. This extra bond removes some of the electron density from the nitrogen atom, leaving it slightly positive. The nitrogen's positive charge would most likely be spread over the other electropositive atoms in the system, such as the hydrogen. As the alkyl groups are electron-donating, this positive charge on the nitrogen, arising from slight electron deficiency, will be stabilised.

== [P(CH3)4]+ ==
===Analysis===

'''Table 21'''
<pre>
Item Value Threshold Converged?
Maximum Force 0.000128 0.000450 YES
RMS Force 0.000032 0.000300 YES
Maximum Displacement 0.000666 0.001800 YES
RMS Displacement 0.000277 0.001200 YES
</pre>

'''Table 22'''
<pre>
Low frequencies --- -0.0036 -0.0009 -0.0002 51.2698 51.2698 51.2699
Low frequencies --- 186.5950 211.3905 211.3905
</pre>

Frequency file: [[Media: IM_SYMM_FREQ_1.LOG | P(CH3)4+_Frequencies.log]]

'''Table 23'''

[[File:IM_P(CH3)4.PNG|300px]]

<jmol><jmolApplet>
<title>optimised NH3BH3 molecule</title>
<color>white</color>
<size>250</size>
<uploadedFileContents>IM_SYMM_FREQ_1.LOG</uploadedFileContents>
<script>frame 1.2</script>
</jmolApplet></jmol>

===Charge Analysis===

'''Figure 7'''

[[File:IM_P(CH3)4_Charges.PNG|300px]]

== Comparisons ==

{| class="wikitable"
|+ Table 24
|-
| [N(CH3)4]+ Charge Distribution || [P(CH3)4]+ Charge DIstribution
|-
| [[File:IM N(CH3)4 Charges.PNG|200px]] || [[File:IM P(CH3)4 Charges.PNG|200px]]
|}

The same colour range (the largest out of both) were used to visualise both molecules, as seen below in Figure 8.

'''Figure 8'''

[[File:IM_NBO_Values.PNG|200px]]

{| class="wikitable"
|+ Table 25
|-
| Atom (in [N(CH3)4]+) || Charge (C) || Atom (in [P(CH3)4]+) || Charge (C)
|-
| N || -0.295 || P || 1.666
|-
| C || -0.483 || C || -1.060
|-
| H || 0.269 || H || 0.298
|}