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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Diethylzinc</id>
	<title>Diethylzinc - Revision history</title>
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	<updated>2026-04-27T07:59:11Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Diethylzinc&amp;diff=6305442&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Diethylzinc&amp;diff=6305442&amp;oldid=prev"/>
		<updated>2025-02-17T01:50:25Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 01:50, 17 February 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l29&quot;&gt;Line 29:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 29:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Reagents]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Reagents]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Chem-stub}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Chem-stub}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:Diethylzinc_structure.svg|Structure of Diethylzinc&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:Diethylzinc-3D-balls.png|3D ball model of Diethylzinc&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=Diethylzinc&amp;diff=5408540&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Diethylzinc&amp;diff=5408540&amp;oldid=prev"/>
		<updated>2024-03-19T05:33:16Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Diethylzinc&amp;#039;&amp;#039;&amp;#039; ([[IUPAC]] name: diethylzinc) is an organozinc compound with the formula Zn(C2H5)2. It is a highly reactive, colorless liquid which is sensitive to air and moisture, making it a challenging substance to work with under standard laboratory conditions. Diethylzinc is used primarily as a reagent in the synthesis of organic compounds and as a precursor to other zinc compounds.&lt;br /&gt;
&lt;br /&gt;
== Properties ==&lt;br /&gt;
Diethylzinc is a volatile, pyrophoric liquid that ignites spontaneously in air. It is soluble in hydrocarbons, ethers, and other organic solvents, but reacts violently with water, alcohols, and acids to produce ethane and zinc salts. The compound has a boiling point of 118°C and a melting point of -28°C.&lt;br /&gt;
&lt;br /&gt;
== Synthesis ==&lt;br /&gt;
Diethylzinc can be synthesized by the reaction of ethyl iodide with zinc metal. This process involves the direct reaction of zinc with ethyl iodide in the presence of anhydrous ether or tetrahydrofuran (THF) under reflux conditions. The reaction is highly exothermic and requires careful control to prevent runaway reactions.&lt;br /&gt;
&lt;br /&gt;
== Applications ==&lt;br /&gt;
Diethylzinc is used in organic synthesis, primarily as a reagent for the introduction of the ethyl group into organic molecules. It acts as a strong nucleophile and can be used in the formation of carbon-zinc bonds. Diethylzinc is also employed in the synthesis of other organozinc compounds and as a reducing agent in certain types of reactions.&lt;br /&gt;
&lt;br /&gt;
In addition to its use in chemical synthesis, diethylzinc has been explored as a potential reagent for the deposition of zinc-containing films in materials science applications, particularly in the area of thin-film semiconductors and nanotechnology.&lt;br /&gt;
&lt;br /&gt;
== Safety ==&lt;br /&gt;
Due to its pyrophoric nature and the potential for violent reaction with water, handling diethylzinc requires strict safety precautions. It should be stored under an inert atmosphere in tightly sealed containers. Protective equipment, including gloves and eye protection, is essential when working with this compound. In case of a spill or accidental exposure, appropriate emergency procedures should be followed to mitigate the risk of fire or chemical burns.&lt;br /&gt;
&lt;br /&gt;
== See also ==&lt;br /&gt;
* [[Organometallic chemistry]]&lt;br /&gt;
* [[Zinc]]&lt;br /&gt;
* [[Ethyl group]]&lt;br /&gt;
* [[Reagent]]&lt;br /&gt;
* [[Thin-film deposition]]&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Organometallic compounds]]&lt;br /&gt;
[[Category:Zinc compounds]]&lt;br /&gt;
[[Category:Reagents]]&lt;br /&gt;
{{Chem-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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