Hexasulfur

Chemical compound From Wikipedia, the free encyclopedia

Hexasulfur is an inorganic chemical with the chemical formula S6. This allotrope of sulfur was first prepared by M. R. Engel in 1891 by treating thiosulfate with HCl.[2] Hexasulfur is orange-red and forms a rhombohedral crystal.[3] It is also called cyclo-S6, ρ-sulfur, ε-sulfur, Engel's sulfur, and Aten's sulfur.[4]

Quick facts Names, Identifiers ...
Hexasulfur
Ball and stick model of hexathiane
Ball and stick model of hexathiane
Names
Systematic IUPAC name
  • Cyclohexasulfane
  • cyclo-Hexasulfur
  • Hexathiane[1]
Other names
Hexasulfur
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/S6/c1-2-4-6-5-3-1 checkY
    Key: FEXCMMPRRBSCRG-UHFFFAOYSA-N checkY
  • S1SSSSS1
Properties
S6
Molar mass 192.36 g·mol−1
Appearance Vivid, orange, opaque crystals
Related compounds
Related compounds
Octasulfur
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Nomenclature

The most common name for the compound is "hexasulfur".

The preferred IUPAC name, cyclohexasulfane, is constructed according to compositional nomenclature.

Hexasulfur is the final member of the thiane heterocyclic series, in which every carbon atom is substituted with a sulfur atom, giving the systematic name "hexathiane", a valid IUPAC name using substitutive nomenclature.

Another valid IUPAC systematic name, cyclo-hexasulfur, is constructed using additive nomenclature.

Structure

Hexasulfur consists of rings of six sulfur atoms. It is thus a simple cyclosulfane and an allotrope of sulfur. Hexasulfur adopts a chair configuration similar to that of cyclohexane, with bond angles of 102.2°. The sulfur atoms are equivalent.[3]

Preparation

A method of preparation involves the reaction of a polysulfane with sulfur monochloride:[3]

H2S4 + S2Cl2cyclo-S6 + 2 HCl (dilute solution in diethyl ether)


References

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