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	<id>https://chemwiki.ch.ic.ac.uk/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Sdc05</id>
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	<updated>2026-04-06T20:53:09Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7729</id>
		<title>It:Osmium Tetroxide</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7729"/>
		<updated>2006-12-07T21:20:52Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;=&lt;br /&gt;
&lt;br /&gt;
Chemical Formula: OsO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
Molar Mass: 254.23 gmol&amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt;&lt;br /&gt;
Melting point: 40°C&lt;br /&gt;
Boiling point: 130°C&lt;br /&gt;
VERY TOXIC Especially to the eyes.&lt;br /&gt;
Colourless/Yellow&lt;br /&gt;
Ozonelike odour&lt;br /&gt;
&lt;br /&gt;
Osmium Tetroxide is an example of the highest oxidation state achieved by transition metal. It has a tetrahedral shape as shown in jmol format below with O=Os=O bond angle of ~109°.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
HEADER    NONAME 07-Dec-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  07-Dec-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       0.000  -1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      2 Os           0      -0.000  -0.000   0.000  0.00  0.00          Os+0&lt;br /&gt;
ATOM      3  O           0       0.000   1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      4  O           0      -1.424   0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      5  O           0       1.424  -0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
CONECT    1    2    0    0    0                                         NONE  10&lt;br /&gt;
CONECT    2    1    3    4    5                                         NONE  11&lt;br /&gt;
CONECT    3    2    0    0    0                                         NONE  12&lt;br /&gt;
CONECT    4    2    0    0    0                                         NONE  13&lt;br /&gt;
CONECT    5    2    0    0    0                                         NONE  14&lt;br /&gt;
END                                                                     NONE  15&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Weapon of terror?===&lt;br /&gt;
Osmium Tetroxide has been seen as a possible terrorist weapon, this is becuase of its possible use as a catalysist in an explosive device, or due to its high toxicity. The catalytic behaviour is possible due to osmium’s many oxidation states, and the toxicity because of its acidic and corrosive nature in aqueous systems. However it&#039;s cost has had it dubbed &#039;the billionaires weapon&#039;.&lt;br /&gt;
&lt;br /&gt;
=Preparation&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;=&lt;br /&gt;
&lt;br /&gt;
Addition of oxygen by burning the metal at 800 °C&lt;br /&gt;
&lt;br /&gt;
[[Image:OsO4.JPG|Thumb|Left|200|Preparation]]&lt;br /&gt;
&lt;br /&gt;
=Use in Organic Chemistry=&lt;br /&gt;
&lt;br /&gt;
Oxidation of C=C bond&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:OsO4 oxidation.JPG|Thumb|Left|200|Reaction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Osmium forms several oxofluorides, all of which are very sensitive to moisture. Purple cis-OsO2F4 forms at 77 K in an aqueous solution of HF&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
OsO4 + 2 KrF2 → cis-OsO2F4 + 2 Kr + O2 &lt;br /&gt;
OsO4 also reacts with F2 to form yellow OsOF2:&lt;br /&gt;
&lt;br /&gt;
2 OsO4 + 2 F2 → 2 OsO3F2 + O2 &lt;br /&gt;
OsO4 reacts with one equivalent of [Me4N]F at 298 K and 2 equivalents at 253 K[4]:&lt;br /&gt;
&lt;br /&gt;
OsO4 + [Me4N]F → [Me4N][OsO4F] &lt;br /&gt;
OsO4 + 2 [Me4N]F → [Me4N]2[cis-OsO4F2]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.http://www.chm.bris.ac.uk/motm/oso4/oso4v.htm&lt;br /&gt;
&lt;br /&gt;
2.http://news.bbc.co.uk/1/hi/uk/3604857.stm&lt;br /&gt;
&lt;br /&gt;
3.Christe et al. Osmium Tetrafluoride Dioxide, cis-OsO2F4. J. Am. Chem. Soc. 1993, 115. 11279-11284&lt;br /&gt;
&lt;br /&gt;
4. http://en.wikipedia.org/wiki/Osmium_tetroxide&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7436</id>
		<title>It:Osmium Tetroxide</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7436"/>
		<updated>2006-12-07T12:09:27Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;=Introduction&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;=&lt;br /&gt;
Chemical Formula: OsO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&lt;br /&gt;
==Physical Properties==&lt;br /&gt;
Melting point: 40°C&lt;br /&gt;
Boiling point: 130°C&lt;br /&gt;
VERY TOXIC Especially to the eyes.&lt;br /&gt;
Colourless/Yellow&lt;br /&gt;
Ozonelike odour&lt;br /&gt;
&lt;br /&gt;
Osmium Tetroxide is an example of the highest oxidation state achieved by transition metal. It has a tetrahedral shape as shown in jmol format below with O=Os=O bond angle of ~109°.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
HEADER    NONAME 07-Dec-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  07-Dec-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       0.000  -1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      2 Os           0      -0.000  -0.000   0.000  0.00  0.00          Os+0&lt;br /&gt;
ATOM      3  O           0       0.000   1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      4  O           0      -1.424   0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      5  O           0       1.424  -0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
CONECT    1    2    0    0    0                                         NONE  10&lt;br /&gt;
CONECT    2    1    3    4    5                                         NONE  11&lt;br /&gt;
CONECT    3    2    0    0    0                                         NONE  12&lt;br /&gt;
CONECT    4    2    0    0    0                                         NONE  13&lt;br /&gt;
CONECT    5    2    0    0    0                                         NONE  14&lt;br /&gt;
END                                                                     NONE  15&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
=Preparation&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;=&lt;br /&gt;
&lt;br /&gt;
Addition of oxygen by burning the metal at 800 °C&lt;br /&gt;
&lt;br /&gt;
[[Image:OsO4.JPG|Thumb|Left|200|Preparation]]&lt;br /&gt;
&lt;br /&gt;
=Use in Organic Chemistry=&lt;br /&gt;
&lt;br /&gt;
Oxidation of C=C bond&lt;br /&gt;
&lt;br /&gt;
[[Image:OsO4 oxidation.JPG|Thumb|Left|200|Reaction]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.http://www.chm.bris.ac.uk/motm/oso4/oso4v.htm&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:OsO4_oxidation.JPG&amp;diff=7435</id>
		<title>File:OsO4 oxidation.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:OsO4_oxidation.JPG&amp;diff=7435"/>
		<updated>2006-12-07T12:07:13Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:OsO4.JPG&amp;diff=7433</id>
		<title>File:OsO4.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:OsO4.JPG&amp;diff=7433"/>
		<updated>2006-12-07T12:00:54Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7419</id>
		<title>It:Osmium Tetroxide</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Osmium_Tetroxide&amp;diff=7419"/>
		<updated>2006-12-07T11:46:09Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
HEADER    NONAME 07-Dec-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  07-Dec-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  O           0       0.000  -1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      2 Os           0      -0.000  -0.000   0.000  0.00  0.00          Os+0&lt;br /&gt;
ATOM      3  O           0       0.000   1.424  -1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      4  O           0      -1.424   0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
ATOM      5  O           0       1.424  -0.000   1.007  0.00  0.00           O+0&lt;br /&gt;
CONECT    1    2    0    0    0                                         NONE  10&lt;br /&gt;
CONECT    2    1    3    4    5                                         NONE  11&lt;br /&gt;
CONECT    3    2    0    0    0                                         NONE  12&lt;br /&gt;
CONECT    4    2    0    0    0                                         NONE  13&lt;br /&gt;
CONECT    5    2    0    0    0                                         NONE  14&lt;br /&gt;
END                                                                     NONE  15&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=7414</id>
		<title>It:projects</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:projects&amp;diff=7414"/>
		<updated>2006-12-07T11:38:19Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Supplemental  Project Page */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__FORCETOC__&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;You MUST use the  Edit buttons on the right to edit this content.  Do NOT use the Edit button on the top of this page.&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
== Sandbox (Play-Pen) ==	 &lt;br /&gt;
		 &lt;br /&gt;
This is an area where you can play without worrying what you do. Enter it by pressing the [Edit] button &#039;&#039;&#039;on the right&#039;&#039;&#039; and &#039;&#039;&#039;not&#039;&#039;&#039; at the top. Go here for a [http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet &#039;&#039;cheat sheet&#039;&#039;] summary of how to create a Wiki page.	 It&#039;s a free-for-all in here! Learn how to use a Wiki by coming here! PS This is how to do Greek: &amp;amp;Alpha;, &amp;amp;alpha;, &amp;amp;beta; &amp;amp;Delta;, &amp;amp;delta;	 		 &lt;br /&gt;
Try copying/pasting some of the [http://www.ch.ic.ac.uk/local/it/lab1.html examples in the course work] into this page. See the effect by selecting &#039;&#039;&#039;Show Preview&#039;&#039;&#039;. No not use &#039;&#039;&#039;Save Page&#039;&#039;&#039; so as to leave this area uncluttered for others.&lt;br /&gt;
----&lt;br /&gt;
{|&lt;br /&gt;
|NEW: This demonstrates the use of  Jmol loading discrete molecule files (rather than having to paste them into the wiki page).  Upload the molecule file, and invoke it as shown here. Use it for eg loading large proteins etc.  Sorry about the delay in getting this working, but the cause was pretty unobvious.--[[User:Rzepa|Rzepa]] 16:07, 4 December 2006 (UTC)&lt;br /&gt;
&amp;lt;center&amp;gt;&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;title&amp;gt;Pentahelicene&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;yellow&amp;lt;/color&amp;gt;&lt;br /&gt;
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&amp;lt;menuHeight&amp;gt;-1&amp;lt;/menuHeight&amp;gt;&lt;br /&gt;
&amp;lt;/jmolMenu&amp;gt;&lt;br /&gt;
&amp;lt;jmolButton&amp;gt;&lt;br /&gt;
    &amp;lt;script&amp;gt;console&amp;lt;/script&amp;gt;&lt;br /&gt;
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&amp;lt;/jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&amp;lt;/center&amp;gt;&lt;br /&gt;
-----&lt;br /&gt;
&amp;lt;center&amp;gt;&amp;lt;jmol&amp;gt;&amp;lt;jmolAppletButton&amp;gt;&amp;lt;title&amp;gt;Show Pentahelicene in popup window&amp;lt;/title&amp;gt;&amp;lt;color&amp;gt;cyan&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;uploadedFileContents&amp;gt;Pentahelicene.mol&amp;lt;/uploadedFileContents&amp;gt;&amp;lt;/jmolAppletButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&amp;lt;/center&amp;gt;&lt;br /&gt;
&lt;br /&gt;
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| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Methoxsalen|Methoxsalen (Treatment of psoriasis)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |15&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Hycocine|Hyoscine (From Mandrake and Witches Henbane, pre-med before surgery)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |16&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Capreomycin|Capreomycin (Drug-resistant TB)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |17&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:wilkinson|Wilkinson&#039;s catalyst]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |18&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Jacobsen|Jacobsen&#039;s epoxidation catalyst]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |19&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Methylaluminoxane|Methylaluminoxane: MAO - hugely important ethylene polymerisation cocatalyst]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |20&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Schwartz|Schwartz reagent for the hydrozirconation of alkenes and alkynes]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |21&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Schrock|Schrock metathesis catalyst]]&lt;br /&gt;
|-&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; |22&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:knots|Molecular-scale knots (nanoscale devices)]]&lt;br /&gt;
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|bgcolor=&amp;quot;#CCFF00&amp;quot; |23&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Vioxx|Vioxx (treatment of osteoarthritis symptoms and pain)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |24&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |25&lt;br /&gt;
| bgcolor=&amp;quot;#CCFF00&amp;quot; | [[it:Ceftriaxone|Ceftriaxone (Gonorrhoea)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |26&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Zithromycin|Zithromycin (anti-infective)]]&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |27&lt;br /&gt;
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| bgcolor=&amp;quot;#CCFF00&amp;quot; |28&lt;br /&gt;
| bgcolor=&amp;quot;#66FF99&amp;quot; | [[it:Cyameluric Acid|Cyameluric acid (Linus Pauling&#039;s last idea!)]]&lt;br /&gt;
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[[R &amp;amp; S Phrases]]&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5738</id>
		<title>It:Schrock</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5738"/>
		<updated>2006-11-20T17:18:46Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
[[Image:Schrock2.jpg|thumb|left|General example, commercially available example&amp;lt;sup&amp;gt;2&amp;lt;sup&amp;gt;]]&lt;br /&gt;
&lt;br /&gt;
This is an important discovery as the catalysts used before were sensitive to air and moisture, created side reactions and were relatively short-lived.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; Schrock&#039;s discovery of the catalysts using tungsten provided one of the first stable metathesis catalyst.&amp;lt;sup&amp;gt;2&amp;lt;sup&amp;gt;&lt;br /&gt;
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&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;400&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
CRYST1   8.5594   6.0337  11.0220  90.00 105.97  90.00     P21/c&lt;br /&gt;
SCALE1      0.116831 -0.000000  0.033428       0.000000&lt;br /&gt;
SCALE2     -0.000000  0.165736 -0.000000       0.000000&lt;br /&gt;
SCALE3     -0.000000  0.000000  0.094368       0.000000&lt;br /&gt;
&lt;br /&gt;
HEADER    NONAME 20-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  20-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0       2.963  -1.542   0.211  0.00  0.00           C+0&lt;br /&gt;
ATOM      2  C           0       1.711  -2.418   0.287  0.00  0.00           C+0&lt;br /&gt;
ATOM      3  C           0       1.225  -2.737  -1.129  0.00  0.00           C+0&lt;br /&gt;
ATOM      4  C           0       2.043  -3.720   1.018  0.00  0.00           C+0&lt;br /&gt;
ATOM      5  O           0       0.685  -1.722   0.997  0.00  0.00           O+0&lt;br /&gt;
ATOM      6  W           0       0.327  -0.023  -0.017  0.00  0.00           W+0&lt;br /&gt;
ATOM      7  N           0      -1.038   0.906   0.803  0.00  0.00           N+0&lt;br /&gt;
ATOM      8  C           0      -2.234   0.351   0.930  0.00  0.00           C+0&lt;br /&gt;
ATOM      9  C           0      -3.290   1.059   1.560  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  C           0      -4.515   0.474   1.682  0.00  0.00           C+0&lt;br /&gt;
ATOM     11  C           0      -4.733  -0.808   1.195  0.00  0.00           C+0&lt;br /&gt;
ATOM     12  C           0      -3.710  -1.515   0.576  0.00  0.00           C+0&lt;br /&gt;
ATOM     13  C           0      -2.475  -0.955   0.432  0.00  0.00           C+0&lt;br /&gt;
ATOM     14  O           0       1.989   1.107  -0.037  0.00  0.00           O+0&lt;br /&gt;
ATOM     15  C           0       1.961   1.904   1.149  0.00  0.00           C+0&lt;br /&gt;
ATOM     16  C           0       1.778   0.998   2.368  0.00  0.00           C+0&lt;br /&gt;
ATOM     17  C           0       3.278   2.673   1.277  0.00  0.00           C+0&lt;br /&gt;
ATOM     18  C           0       0.798   2.895   1.070  0.00  0.00           C+0&lt;br /&gt;
ATOM     19  C           0      -0.176  -0.444  -1.804  0.00  0.00           C+0&lt;br /&gt;
ATOM     20  C           0      -0.600   0.653  -2.746  0.00  0.00           C+0&lt;br /&gt;
ATOM     21  C           0      -0.395   2.011  -2.072  0.00  0.00           C+0&lt;br /&gt;
ATOM     22  C           0       0.243   0.584  -4.021  0.00  0.00           C+0&lt;br /&gt;
ATOM     23  C           0      -2.078   0.478  -3.101  0.00  0.00           C+0&lt;br /&gt;
ATOM     24  H           0       2.744  -0.644  -0.367  0.00  0.00           H+0&lt;br /&gt;
ATOM     25  H           0       3.270  -1.260   1.217  0.00  0.00           H+0&lt;br /&gt;
ATOM     26  H           0       3.766  -2.098  -0.272  0.00  0.00           H+0&lt;br /&gt;
ATOM     27  H           0       1.773  -3.596  -1.516  0.00  0.00           H+0&lt;br /&gt;
ATOM     28  H           0       0.160  -2.967  -1.104  0.00  0.00           H+0&lt;br /&gt;
ATOM     29  H           0       1.396  -1.876  -1.774  0.00  0.00           H+0&lt;br /&gt;
ATOM     30  H           0       2.389  -3.493   2.026  0.00  0.00           H+0&lt;br /&gt;
ATOM     31  H           0       1.151  -4.344   1.072  0.00  0.00           H+0&lt;br /&gt;
ATOM     32  H           0       2.826  -4.251   0.476  0.00  0.00           H+0&lt;br /&gt;
ATOM     33  H           0      -3.123   2.056   1.940  0.00  0.00           H+0&lt;br /&gt;
ATOM     34  H           0      -5.321   1.010   2.162  0.00  0.00           H+0&lt;br /&gt;
ATOM     35  H           0      -5.708  -1.261   1.298  0.00  0.00           H+0&lt;br /&gt;
ATOM     36  H           0      -3.894  -2.512   0.202  0.00  0.00           H+0&lt;br /&gt;
ATOM     37  H           0      -1.681  -1.507  -0.049  0.00  0.00           H+0&lt;br /&gt;
ATOM     38  H           0       2.649   0.351   2.473  0.00  0.00           H+0&lt;br /&gt;
ATOM     39  H           0       1.670   1.610   3.263  0.00  0.00           H+0&lt;br /&gt;
ATOM     40  H           0       0.885   0.387   2.236  0.00  0.00           H+0&lt;br /&gt;
ATOM     41  H           0       3.408   3.318   0.409  0.00  0.00           H+0&lt;br /&gt;
ATOM     42  H           0       3.257   3.280   2.182  0.00  0.00           H+0&lt;br /&gt;
ATOM     43  H           0       4.107   1.967   1.333  0.00  0.00           H+0&lt;br /&gt;
ATOM     44  H           0      -0.135   2.378   1.296  0.00  0.00           H+0&lt;br /&gt;
ATOM     45  H           0       0.953   3.696   1.793  0.00  0.00           H+0&lt;br /&gt;
ATOM     46  H           0       0.746   3.316   0.066  0.00  0.00           H+0&lt;br /&gt;
ATOM     47  H           0      -0.158  -1.470  -2.142  0.00  0.00           H+0&lt;br /&gt;
ATOM     48  H           0       0.658   2.136  -1.818  0.00  0.00           H+0&lt;br /&gt;
ATOM     49  H           0      -0.702   2.805  -2.753  0.00  0.00           H+0&lt;br /&gt;
ATOM     50  H           0      -0.996   2.060  -1.163  0.00  0.00           H+0&lt;br /&gt;
ATOM     51  H           0       0.032  -0.348  -4.546  0.00  0.00           H+0&lt;br /&gt;
ATOM     52  H           0      -0.004   1.428  -4.665  0.00  0.00           H+0&lt;br /&gt;
ATOM     53  H           0       1.300   0.623  -3.760  0.00  0.00           H+0&lt;br /&gt;
ATOM     54  H           0      -2.678   0.527  -2.192  0.00  0.00           H+0&lt;br /&gt;
ATOM     55  H           0      -2.384   1.271  -3.782  0.00  0.00           H+0&lt;br /&gt;
ATOM     56  H           0      -2.224  -0.490  -3.581  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   24   25   26                                         NONE  61&lt;br /&gt;
CONECT    2    1    3    4    5                                         NONE  62&lt;br /&gt;
CONECT    3    2   27   28   29                                         NONE  63&lt;br /&gt;
CONECT    4    2   30   31   32                                         NONE  64&lt;br /&gt;
CONECT    5    2    6    0    0                                         NONE  65&lt;br /&gt;
CONECT    6    5    7   14   19                                         NONE  66&lt;br /&gt;
CONECT    7    6    8    0    0                                         NONE  67&lt;br /&gt;
CONECT    8    7   13    9    0                                         NONE  68&lt;br /&gt;
CONECT    9    8   10   33    0                                         NONE  69&lt;br /&gt;
CONECT   10    9   11   34    0                                         NONE  70&lt;br /&gt;
CONECT   11   10   12   35    0                                         NONE  71&lt;br /&gt;
CONECT   12   11   13   36    0                                         NONE  72&lt;br /&gt;
CONECT   13   12    8   37    0                                         NONE  73&lt;br /&gt;
CONECT   14    6   15    0    0                                         NONE  74&lt;br /&gt;
CONECT   15   14   16   17   18                                         NONE  75&lt;br /&gt;
CONECT   16   15   38   39   40                                         NONE  76&lt;br /&gt;
CONECT   17   15   41   42   43                                         NONE  77&lt;br /&gt;
CONECT   18   15   44   45   46                                         NONE  78&lt;br /&gt;
CONECT   19    6   20   47    0                                         NONE  79&lt;br /&gt;
CONECT   20   19   21   22   23                                         NONE  80&lt;br /&gt;
CONECT   21   20   48   49   50                                         NONE  81&lt;br /&gt;
CONECT   22   20   51   52   53                                         NONE  82&lt;br /&gt;
CONECT   23   20   54   55   56                                         NONE  83&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
An example of Schrock Metathesis catalyst in 3-D.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Reference&lt;br /&gt;
&lt;br /&gt;
1.http://www.rsc.org/chemistryworld/restricted/2005/November/prize.asp&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5736</id>
		<title>It:Schrock</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5736"/>
		<updated>2006-11-20T17:11:05Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
[[Image:Schrock2.jpg|thumb|left|General example, commercially available example&amp;lt;sup&amp;gt;2&amp;lt;sup&amp;gt;]]&lt;br /&gt;
&lt;br /&gt;
This is an important discovery as the catalysts used before were sensitive to air and moisture, created side reactions and were relatively short-lived.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; Schrock&#039;s discovery of the catalysts using tungsten provided one of the first stable metathesis catalyst.&amp;lt;sup&amp;gt;2&amp;lt;sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Reference&lt;br /&gt;
&lt;br /&gt;
1.http://www.rsc.org/chemistryworld/restricted/2005/November/prize.asp&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Schrock2.jpg&amp;diff=5735</id>
		<title>File:Schrock2.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Schrock2.jpg&amp;diff=5735"/>
		<updated>2006-11-20T17:01:18Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5734</id>
		<title>It:Schrock</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Schrock&amp;diff=5734"/>
		<updated>2006-11-20T17:01:06Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
&lt;br /&gt;
[[image:schrock.JPG|thumb|left|200|schrock]]&lt;br /&gt;
From reference 1.&lt;br /&gt;
&lt;br /&gt;
This is an important discovery as the catalysts used before were sensitive to air and moisture, created side reactions and were relatively short-lived.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Reference&lt;br /&gt;
1.http://www.strem.com/code/technical_notes/74-1800tech.pdf&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Schrock.JPG&amp;diff=5724</id>
		<title>File:Schrock.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Schrock.JPG&amp;diff=5724"/>
		<updated>2006-11-20T16:43:35Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5709</id>
		<title>It:knots</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5709"/>
		<updated>2006-11-20T16:26:54Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* knots */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===knots===&lt;br /&gt;
&lt;br /&gt;
[[Image:knots.jpg|thumb|left|300|reference1]]&lt;br /&gt;
The simplest knotted molecule so far.&lt;br /&gt;
&lt;br /&gt;
Reference&lt;br /&gt;
1. http://plus.maths.org/issue15/features/knots/index.html&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5674</id>
		<title>It:knots</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5674"/>
		<updated>2006-11-20T15:53:14Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===knots===&lt;br /&gt;
&lt;br /&gt;
[[Image:knots.jpg|thumb|left|300|reference1]]&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5673</id>
		<title>It:knots</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:knots&amp;diff=5673"/>
		<updated>2006-11-20T15:52:56Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===knots===&lt;br /&gt;
&lt;br /&gt;
[[Image:knots.jpg|thumb|left|300|reference 1]&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:Knots.jpg&amp;diff=5666</id>
		<title>File:Knots.jpg</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:Knots.jpg&amp;diff=5666"/>
		<updated>2006-11-20T15:48:10Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5661</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5661"/>
		<updated>2006-11-20T15:43:57Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;100&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
CRYST1   8.5594   6.0337  11.0220  90.00 105.97  90.00     P21/c&lt;br /&gt;
SCALE1      0.116831 -0.000000  0.033428       0.000000&lt;br /&gt;
SCALE2     -0.000000  0.165736 -0.000000       0.000000&lt;br /&gt;
SCALE3     -0.000000  0.000000  0.094368       0.000000&lt;br /&gt;
HEADER    NONAME 20-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  20-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -0.663   2.118   1.018  0.00  0.00           C+0&lt;br /&gt;
ATOM      2 Al           0      -0.174   0.786  -0.261  0.00  0.00          Al+0&lt;br /&gt;
ATOM      3  O           0       1.449   0.775  -0.942  0.00  0.00           O+0&lt;br /&gt;
ATOM      4 Al           0       2.401  -0.344   0.028  0.00  0.00          Al+0&lt;br /&gt;
ATOM      5  O           0       1.628  -1.282   1.301  0.00  0.00           O+0&lt;br /&gt;
ATOM      6  C           0       4.272  -0.539  -0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  O           0      -1.345  -0.430  -0.757  0.00  0.00           O+0&lt;br /&gt;
ATOM      8 Al           0      -2.830  -0.097   0.127  0.00  0.00          Al+0&lt;br /&gt;
ATOM      9  C           0      -4.364  -1.204  -0.131  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  H           0       0.210   2.723   1.265  0.00  0.00           H+0&lt;br /&gt;
ATOM     11  H           0      -1.440   2.757   0.598  0.00  0.00           H+0&lt;br /&gt;
ATOM     12  H           0      -1.038   1.635   1.920  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       4.568   0.117  -1.118  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       4.828  -0.272   0.599  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       4.488  -1.573  -0.567  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -4.667  -1.167  -1.178  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -4.121  -2.231   0.140  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -5.181  -0.846   0.496  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   10   11   12                                         NONE  23&lt;br /&gt;
CONECT    2    1    3    7    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4    0    0                                         NONE  25&lt;br /&gt;
CONECT    4    3    5    6    0                                         NONE  26&lt;br /&gt;
CONECT    5    4    0    0    0                                         NONE  27&lt;br /&gt;
CONECT    6    4   13   14   15                                         NONE  28&lt;br /&gt;
CONECT    7    2    8    0    0                                         NONE  29&lt;br /&gt;
CONECT    8    7    9    0    0                                         NONE  30&lt;br /&gt;
CONECT    9    8   16   17   18                                         NONE  31&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5660</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5660"/>
		<updated>2006-11-20T15:43:18Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Structure */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5659</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5659"/>
		<updated>2006-11-20T15:42:56Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Structure */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
CRYST1   8.5594   6.0337  11.0220  90.00 105.97  90.00     P21/c&lt;br /&gt;
SCALE1      0.116831 -0.000000  0.033428       0.000000&lt;br /&gt;
SCALE2     -0.000000  0.165736 -0.000000       0.000000&lt;br /&gt;
SCALE3     -0.000000  0.000000  0.094368       0.000000&lt;br /&gt;
HEADER    NONAME 20-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  20-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -0.663   2.118   1.018  0.00  0.00           C+0&lt;br /&gt;
ATOM      2 Al           0      -0.174   0.786  -0.261  0.00  0.00          Al+0&lt;br /&gt;
ATOM      3  O           0       1.449   0.775  -0.942  0.00  0.00           O+0&lt;br /&gt;
ATOM      4 Al           0       2.401  -0.344   0.028  0.00  0.00          Al+0&lt;br /&gt;
ATOM      5  O           0       1.628  -1.282   1.301  0.00  0.00           O+0&lt;br /&gt;
ATOM      6  C           0       4.272  -0.539  -0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  O           0      -1.345  -0.430  -0.757  0.00  0.00           O+0&lt;br /&gt;
ATOM      8 Al           0      -2.830  -0.097   0.127  0.00  0.00          Al+0&lt;br /&gt;
ATOM      9  C           0      -4.364  -1.204  -0.131  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  H           0       0.210   2.723   1.265  0.00  0.00           H+0&lt;br /&gt;
ATOM     11  H           0      -1.440   2.757   0.598  0.00  0.00           H+0&lt;br /&gt;
ATOM     12  H           0      -1.038   1.635   1.920  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       4.568   0.117  -1.118  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       4.828  -0.272   0.599  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       4.488  -1.573  -0.567  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -4.667  -1.167  -1.178  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -4.121  -2.231   0.140  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -5.181  -0.846   0.496  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   10   11   12                                         NONE  23&lt;br /&gt;
CONECT    2    1    3    7    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4    0    0                                         NONE  25&lt;br /&gt;
CONECT    4    3    5    6    0                                         NONE  26&lt;br /&gt;
CONECT    5    4    0    0    0                                         NONE  27&lt;br /&gt;
CONECT    6    4   13   14   15                                         NONE  28&lt;br /&gt;
CONECT    7    2    8    0    0                                         NONE  29&lt;br /&gt;
CONECT    8    7    9    0    0                                         NONE  30&lt;br /&gt;
CONECT    9    8   16   17   18                                         NONE  31&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5657</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5657"/>
		<updated>2006-11-20T15:42:09Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Structure */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
CRYST1   8.5594   6.0337  11.0220  90.00 105.97  90.00     P21/c&lt;br /&gt;
SCALE1      0.116831 -0.000000  0.033428       0.000000&lt;br /&gt;
SCALE2     -0.000000  0.165736 -0.000000       0.000000&lt;br /&gt;
SCALE3     -0.000000  0.000000  0.094368       0.000000&lt;br /&gt;
HEADER    NONAME 20-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  20-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -0.663   2.118   1.018  0.00  0.00           C+0&lt;br /&gt;
ATOM      2 Al           0      -0.174   0.786  -0.261  0.00  0.00          Al+0&lt;br /&gt;
ATOM      3  O           0       1.449   0.775  -0.942  0.00  0.00           O+0&lt;br /&gt;
ATOM      4 Al           0       2.401  -0.344   0.028  0.00  0.00          Al+0&lt;br /&gt;
ATOM      5  O           0       1.628  -1.282   1.301  0.00  0.00           O+0&lt;br /&gt;
ATOM      6  C           0       4.272  -0.539  -0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  O           0      -1.345  -0.430  -0.757  0.00  0.00           O+0&lt;br /&gt;
ATOM      8 Al           0      -2.830  -0.097   0.127  0.00  0.00          Al+0&lt;br /&gt;
ATOM      9  C           0      -4.364  -1.204  -0.131  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  H           0       0.210   2.723   1.265  0.00  0.00           H+0&lt;br /&gt;
ATOM     11  H           0      -1.440   2.757   0.598  0.00  0.00           H+0&lt;br /&gt;
ATOM     12  H           0      -1.038   1.635   1.920  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       4.568   0.117  -1.118  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       4.828  -0.272   0.599  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       4.488  -1.573  -0.567  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -4.667  -1.167  -1.178  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -4.121  -2.231   0.140  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -5.181  -0.846   0.496  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   10   11   12                                         NONE  23&lt;br /&gt;
CONECT    2    1    3    7    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4    0    0                                         NONE  25&lt;br /&gt;
CONECT    4    3    5    6    0                                         NONE  26&lt;br /&gt;
CONECT    5    4    0    0    0                                         NONE  27&lt;br /&gt;
CONECT    6    4   13   14   15                                         NONE  28&lt;br /&gt;
CONECT    7    2    8    0    0                                         NONE  29&lt;br /&gt;
CONECT    8    7    9    0    0                                         NONE  30&lt;br /&gt;
CONECT    9    8   16   17   18                                         NONE  31&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5656</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5656"/>
		<updated>2006-11-20T15:41:55Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Properties */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5655</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=5655"/>
		<updated>2006-11-20T15:41:17Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Properties */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane or MAO [(-Al(CH3)O-)n] is a white solid. It is primarily used as a catalyst component in the Ziegler-Natta systems for olefin polymerization.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
MAO reacts vigorously with any chemical with an acidic proton. It is highly soluble in hydrocarbon and hence it is usually used as a solution.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Methylaluminoxane.gif|thumb|center|200|Structure of Methylaluminoxane]]&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
MAO is a complex mixture of linear and cyclic oligomeric aluminxanes containing 20-30 wt. % trimethylalumnium. MAO is pyrophoric meaning it ignites spontaneously since its autoignition is below the room temperature. It has a high solubility in aromatic hydrocarbons such as toluene, xylene, cumene and mesitylene. In aliphatic hydrocarbons it has a lower solubility. This property depends on its Mr, composition and trimethylaluminium content.&lt;br /&gt;
[http://www.albemarle.com/acrofiles/sc2008f_MAO_datasheet.pdf]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;size&amp;gt;200&amp;lt;/size&amp;gt;&lt;br /&gt;
&amp;lt;color&amp;gt;white&amp;lt;/color&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;zoom 100; cpk on;frame 1; move 10 -20 10 0 0 0 0 0 3; delay 1;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;inlineContents&amp;gt;HEADER    CSD ENTRY XICKAV&lt;br /&gt;
CRYST1   8.5594   6.0337  11.0220  90.00 105.97  90.00     P21/c&lt;br /&gt;
SCALE1      0.116831 -0.000000  0.033428       0.000000&lt;br /&gt;
SCALE2     -0.000000  0.165736 -0.000000       0.000000&lt;br /&gt;
SCALE3     -0.000000  0.000000  0.094368       0.000000&lt;br /&gt;
HEADER    NONAME 20-Nov-06                                              NONE   1&lt;br /&gt;
TITLE                                                                   NONE   2&lt;br /&gt;
AUTHOR    WWW daemon apache                                             NONE   3&lt;br /&gt;
REVDAT   1  20-Nov-06     0                                             NONE   4&lt;br /&gt;
ATOM      1  C           0      -0.663   2.118   1.018  0.00  0.00           C+0&lt;br /&gt;
ATOM      2 Al           0      -0.174   0.786  -0.261  0.00  0.00          Al+0&lt;br /&gt;
ATOM      3  O           0       1.449   0.775  -0.942  0.00  0.00           O+0&lt;br /&gt;
ATOM      4 Al           0       2.401  -0.344   0.028  0.00  0.00          Al+0&lt;br /&gt;
ATOM      5  O           0       1.628  -1.282   1.301  0.00  0.00           O+0&lt;br /&gt;
ATOM      6  C           0       4.272  -0.539  -0.300  0.00  0.00           C+0&lt;br /&gt;
ATOM      7  O           0      -1.345  -0.430  -0.757  0.00  0.00           O+0&lt;br /&gt;
ATOM      8 Al           0      -2.830  -0.097   0.127  0.00  0.00          Al+0&lt;br /&gt;
ATOM      9  C           0      -4.364  -1.204  -0.131  0.00  0.00           C+0&lt;br /&gt;
ATOM     10  H           0       0.210   2.723   1.265  0.00  0.00           H+0&lt;br /&gt;
ATOM     11  H           0      -1.440   2.757   0.598  0.00  0.00           H+0&lt;br /&gt;
ATOM     12  H           0      -1.038   1.635   1.920  0.00  0.00           H+0&lt;br /&gt;
ATOM     13  H           0       4.568   0.117  -1.118  0.00  0.00           H+0&lt;br /&gt;
ATOM     14  H           0       4.828  -0.272   0.599  0.00  0.00           H+0&lt;br /&gt;
ATOM     15  H           0       4.488  -1.573  -0.567  0.00  0.00           H+0&lt;br /&gt;
ATOM     16  H           0      -4.667  -1.167  -1.178  0.00  0.00           H+0&lt;br /&gt;
ATOM     17  H           0      -4.121  -2.231   0.140  0.00  0.00           H+0&lt;br /&gt;
ATOM     18  H           0      -5.181  -0.846   0.496  0.00  0.00           H+0&lt;br /&gt;
CONECT    1    2   10   11   12                                         NONE  23&lt;br /&gt;
CONECT    2    1    3    7    0                                         NONE  24&lt;br /&gt;
CONECT    3    2    4    0    0                                         NONE  25&lt;br /&gt;
CONECT    4    3    5    6    0                                         NONE  26&lt;br /&gt;
CONECT    5    4    0    0    0                                         NONE  27&lt;br /&gt;
CONECT    6    4   13   14   15                                         NONE  28&lt;br /&gt;
CONECT    7    2    8    0    0                                         NONE  29&lt;br /&gt;
CONECT    8    7    9    0    0                                         NONE  30&lt;br /&gt;
CONECT    9    8   16   17   18                                         NONE  31&lt;br /&gt;
END&amp;lt;/inlineContents&amp;gt;&lt;br /&gt;
&amp;lt;/jmolApplet&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3171</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3171"/>
		<updated>2006-10-22T16:24:47Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* METHYLALUMINOXANE: */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;= METHYLALUMINOXANE: =&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
==Introduction==&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3170</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3170"/>
		<updated>2006-10-22T16:19:30Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* METHYLALUMINOXANE: */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;= METHYLALUMINOXANE: =&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3168</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3168"/>
		<updated>2006-10-22T15:14:42Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* Activating the catalyst */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;= METHYLALUMINOXANE: =&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This equation illustrates the possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3167</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3167"/>
		<updated>2006-10-22T15:13:31Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: /* METHYLALUMINOXANE: */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;= METHYLALUMINOXANE: =&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound.&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt; Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria.&amp;lt;sup&amp;gt;2&amp;lt;/sup&amp;gt; The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Proposed mechanisms for its uses==&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&amp;lt;sup&amp;gt;5&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
It is generally believed that MAO alkylates and then activates the metal-chloride pre-catalyst species, forming an ion pair which should allow ethene insertion.&amp;lt;sup&amp;gt;4&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:MAO2.JPG]]&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Possible role of the product cation as a catalyst in olefin polymerisation&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
1.Mason, M. R.; Smith, J. M.; Bott, S. G.; Barron, A. R. J. Am. Chem. Soc. 1993, 115, 4971&lt;br /&gt;
2.E. Zurek, T. K. Woo, T. K. Firman, T. Ziegler, Inorg. Chem. 2001, 40, 361-370&lt;br /&gt;
3.S. Srinivasa Reddy, K. Radhakrishnan, S. Sivaram, Polymer Bulletin. 1996, 36, 165-171&lt;br /&gt;
4.http://en.wikipedia.org/wiki/Methylaluminoxane&lt;br /&gt;
5.Sinn, H.; Kaminsky, W.; Vollmer, H. J.; Woldt, R. Angew. Chem. 1980, 92, 396&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:MAO2.JPG&amp;diff=3165</id>
		<title>File:MAO2.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:MAO2.JPG&amp;diff=3165"/>
		<updated>2006-10-22T15:02:12Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3164</id>
		<title>It:Methylaluminoxane</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=It:Methylaluminoxane&amp;diff=3164"/>
		<updated>2006-10-22T14:55:00Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== METHYLALUMINOXANE: ==&lt;br /&gt;
&lt;br /&gt;
Methylaluminoxane, also known as MAO, is mostly used as an important cocatalyst for Ziegler-Natta polymerisations of alkenes.&lt;br /&gt;
&lt;br /&gt;
===Structure===&lt;br /&gt;
The precise structure of Methylaluminoxane is largely unknown as it is not possible to isolate the crystalline sample of this compound. Also, NMR studies of this compound is hindered by disproportionation reactions at high temperatures and association in solution yielding a mixture of different oligomers with multiple equilibria. The general chemical formula of this compound is (-Al(CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;)O-)&amp;lt;sub&amp;gt;n&amp;lt;/sub&amp;gt; where Oxygen joins two aluminium atoms that still bear a CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; group.&lt;br /&gt;
&lt;br /&gt;
===Synthesis===&lt;br /&gt;
MAO is generally prepared by partial hydrolysis of trimethylaluminum, TMA. This is done using hydrated salt dispersed in toluene. Depending on the nature of the salt used and the reaction conditions, MAO with widely differing activities as cocatalysts in polymerization of ethylene is formed.&lt;br /&gt;
&lt;br /&gt;
===Activating the catalyst===&lt;br /&gt;
[[Image:MAOactivator.JPG]]&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
	<entry>
		<id>https://chemwiki.ch.ic.ac.uk/index.php?title=File:MAOactivator.JPG&amp;diff=3163</id>
		<title>File:MAOactivator.JPG</title>
		<link rel="alternate" type="text/html" href="https://chemwiki.ch.ic.ac.uk/index.php?title=File:MAOactivator.JPG&amp;diff=3163"/>
		<updated>2006-10-22T14:36:13Z</updated>

		<summary type="html">&lt;p&gt;Sdc05: It is believed that MAO acts as a cocatalyst by activating the catalyst through this kind of reaction&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;It is believed that MAO acts as a cocatalyst by activating the catalyst through this kind of reaction&lt;/div&gt;</summary>
		<author><name>Sdc05</name></author>
	</entry>
</feed>