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	<title>Selenium hexasulfide - Revision history</title>
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	<updated>2026-05-10T06:50:14Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>imported&gt;Bernardirfan: Clarification</title>
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		<updated>2024-01-27T18:56:45Z</updated>

		<summary type="html">&lt;p&gt;Clarification&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{chembox&lt;br /&gt;
| Watchedfields = changed&lt;br /&gt;
| verifiedrevid = 427848433&lt;br /&gt;
| Name = Selenium hexasulfide&lt;br /&gt;
| OtherNames = {{ubl|Diselenacyclooctasulfane|Diselenaoctathiocane|Diselenium hexasulfide}}&lt;br /&gt;
| Reference = &amp;lt;ref name=&amp;quot;hand&amp;quot;&amp;gt;&lt;br /&gt;
{{Citation|last = Lide|first = David R.|author-link =|year = 1998|title = Handbook of Chemistry and Physics|edition = 87|volume =|series =|location = Boca Raton, Florida|publisher = CRC Press|id =|isbn = 0-8493-0594-2|doi =|oclc =|pages = 4–81|url =}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
| ImageFileL1 = 1,2-Selenium hexasulfide.png&lt;br /&gt;
| ImageCaptionL1 = 1,2-Selenium&amp;lt;br&amp;gt;hexasulfide&lt;br /&gt;
| ImageSizeL1 = 105&amp;lt;!-- allotrope images have unequal widths; we want equal appearance here --&amp;gt;&lt;br /&gt;
| ImageFileR1 = 1,3-Selenium hexasulfide.png&lt;br /&gt;
| ImageCaptionR1 = 1,3-Selenium&amp;lt;br&amp;gt;hexasulfide&lt;br /&gt;
| ImageSizeR1 = 114&lt;br /&gt;
| ImageFileL2 = 1,4-Selenium hexasulfide.png&lt;br /&gt;
| ImageCaptionL2 = 1,4-Selenium&amp;lt;br&amp;gt;hexasulfide&lt;br /&gt;
| ImageSizeL2 = 114&lt;br /&gt;
| ImageFileR2 = 1,5-Selenium hexasulfide.png&lt;br /&gt;
| ImageCaptionR2 = 1,5-Selenium&amp;lt;br&amp;gt;hexasulfide&lt;br /&gt;
| ImageSizeR2 = 105&lt;br /&gt;
|Section1={{Chembox Identifiers&lt;br /&gt;
| index1_label=1,2&lt;br /&gt;
| index5_label=1,5&lt;br /&gt;
| CASNo_Ref = {{cascite|correct|??}}&lt;br /&gt;
| CASNo = 75926-26-0&lt;br /&gt;
| ChemSpiderID1 = 9296780&lt;br /&gt;
| ChemSpiderID5 = 9057901&lt;br /&gt;
| PubChem1 = 11121651&lt;br /&gt;
| PubChem5 = 10882632&lt;br /&gt;
| InChI1=1S/S6Se2/c1-2-4-6-8-7-5-3-1&lt;br /&gt;
| InChIKey1 = GVMSZJKNEHYJTG-UHFFFAOYSA-N&lt;br /&gt;
| SMILES1 = S1SSS[Se][Se]SS1&lt;br /&gt;
| InChI5=1S/S6Se2/c1-3-7-5-2-6-8-4-1&lt;br /&gt;
| InChIKey5 = XHXZYRZXIYIDIG-UHFFFAOYSA-N&lt;br /&gt;
| SMILES5 = S1S[Se]SSS[Se]S1&lt;br /&gt;
  }}&lt;br /&gt;
|Section2={{Chembox Properties&lt;br /&gt;
| Formula = {{chem2|Se2S6}}&lt;br /&gt;
| Se=2|S=6&lt;br /&gt;
| Appearance = orange needles&lt;br /&gt;
| Density = 2.44 g/cm&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt;&lt;br /&gt;
| Solubility =&lt;br /&gt;
| SolubleOther = soluble in [[carbon disulfide]]&lt;br /&gt;
| MeltingPtC = 121.5&lt;br /&gt;
| BoilingPt =&lt;br /&gt;
  }}&lt;br /&gt;
|Section3={{Chembox Structure&lt;br /&gt;
| CrystalStruct =&lt;br /&gt;
  }}&lt;br /&gt;
|Section7={{Chembox Hazards&lt;br /&gt;
  }}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Selenium hexasulfide&amp;#039;&amp;#039;&amp;#039; is a [[chemical compound]] with the [[chemical formula]] {{chem2|Se2S6}}. Its molecular structure is an 8-membered ring, consisting of two [[selenium]] and six [[sulfur]] atoms (&amp;#039;&amp;#039;&amp;#039;diselenacyclooctasulfane&amp;#039;&amp;#039;&amp;#039;), analogous to the {{chem2|S8}} ring, an [[allotrope]] of sulfur ([[cyclooctasulfur]] or cyclooctasulfane), and other 8-membered rings of selenium [[sulfide]]s with formula {{chem2|Se_{&amp;#039;&amp;#039;n&amp;#039;&amp;#039;}S_{8−&amp;#039;&amp;#039;n&amp;#039;&amp;#039;}|}}.&amp;lt;ref name=laitinen/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
There are several [[isomer]]s depending on the relative placement of the selenium atoms in the ring: &amp;#039;&amp;#039;&amp;#039;1,2-diselenacyclooctasulfane&amp;#039;&amp;#039;&amp;#039; (with the two Se atoms adjacent), &amp;#039;&amp;#039;&amp;#039;1,3-diselenacyclooctasulfane&amp;#039;&amp;#039;&amp;#039;, &amp;#039;&amp;#039;&amp;#039;1,4-diselenacyclooctasulfane&amp;#039;&amp;#039;&amp;#039;, and &amp;#039;&amp;#039;&amp;#039;1,5-diselenacyclooctasulfane&amp;#039;&amp;#039;&amp;#039; (with the Se atoms opposite).&amp;lt;ref name=maan&amp;gt;Arto Maaninen, Tristram Chivers, Masood Parvez, Jarkko Pietikäinen, and Risto S. Laitinen (1999), &amp;quot;Syntheses of THF Solutions of SeX&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; (X = Cl, Br) and a New Route to Selenium Sulfides Se&amp;lt;sub&amp;gt;&amp;#039;&amp;#039;n&amp;#039;&amp;#039;&amp;lt;/sub&amp;gt;S&amp;lt;sub&amp;gt;8−&amp;#039;&amp;#039;n&amp;#039;&amp;#039;&amp;lt;/sub&amp;gt; (&amp;#039;&amp;#039;n&amp;#039;&amp;#039; = 1−5): X-ray Crystal Structures of SeCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;(tht)&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and SeCl&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;·tmtu&amp;quot;. &amp;#039;&amp;#039;Inorganic Chemistry&amp;#039;&amp;#039;, volume 38, issue 18, pages 4093–4097. {{doi|10.1021/ic981430h}}&amp;lt;/ref&amp;gt; It is an oxidizing agent.&lt;br /&gt;
&lt;br /&gt;
The 1,2 isomer can be prepared by reaction of [[Sulfur chloride|chlorosulfanes]] and [[dichlorodiselane]] with [[potassium iodide]] in [[carbon disulfide]]. The reaction produces also [[cyclooctaselenium]] {{chem2|Se8}} and all other eight-member [[Cyclic compound|cyclic]] selenium sulfides, except selenacyclooctasulfane {{chem2|SeS7}}, and several six- and seven-membered rings.&amp;lt;ref name=laitinen&amp;gt;Risto S. Laitinen, Pentti Pekone, Yrjö Hiltunen and Tapanin A. Pakkanen (1989), &amp;quot;The &amp;lt;sup&amp;gt;77&amp;lt;/sup&amp;gt;S NMR spestroscopic Identification of Heterocyclic Selenium Sulfides Prepared by the Reactions of Chlorosulfanes and Dichlorodiselane with Potassium Iodide&amp;quot;. &amp;#039;&amp;#039;Acta Chemica Scandinavica&amp;#039;&amp;#039;, volume 43, pages 436-440. {{doi|10.3891/acta.chem.scand.43-0436}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist}}&lt;br /&gt;
&lt;br /&gt;
{{Selenium compounds}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Sulfides]]&lt;br /&gt;
[[Category:Selenium compounds]]&lt;br /&gt;
[[Category:Oxidizing agents]]&lt;br /&gt;
[[Category:Interchalcogens]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{inorganic-compound-stub}}&lt;/div&gt;</summary>
		<author><name>imported&gt;Bernardirfan</name></author>
	</entry>
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