Draft:Xenocycloheptatrisulfurane
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Finished drafting? or |
 | This article possibly contains original research. (March 2025) |
| Names | |
|---|---|
| Other names
Hypothetical compound
| |
| Properties | |
| XeC7H8S3 (speculative) | |
| Molar mass | ~319 g/mol (speculative) |
| Appearance | Unknown, likely unstable at room temperature |
| Melting point | Requires refrigeration to remain stable |
| Structure | |
| Hypothetical compound with a cycloheptatriene ring, three sulfur atoms, and xenon, possibly in a sulfurane-like configuration | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
|
Likely unstable and reactive |
| Related compounds | |
Related compounds
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Cycloheptatriene, Xenon, Sulfurane compounds |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Comment: This article is unsuitable for Wikipedia as it is original research and particularly obscure. As an expert on sulfur chemistry (not that it matters), I love weird stuff with lots of sulfur. But even with that bias, this article is not worth much consideration because the links to any real chemistry is so weak. Xenon sulfides: no. Xenon cycloheptatriene or cycloheptatrienyl: no. The article, no doubt well-intentioned, appears to reflects musings unanchored to real chemistry. User:Smokefoot
Xenocycloheptatrisulfurane is an elusive chemical compound. It is a hypothetical or niche compound coupling a noble gas xenon to a cycloheptatriene ring and to sulfur atoms in a hypothetical complex compound. The structure is a seven-carbon ring of cycloheptatriene with three double bonds and with three sulfur atoms integrated in it maybe as a sulfurane compound, although there is no reference to this compound to be found in common chemical literature. Xenon is an inert and will bind with electronegative atoms like sulfur, The compound is usually unstable on room temperature and need to be refrigerated to stay stable. Cycloheptatriene is a non-aromatic molecule with chemical composition C7H8 and only makes things more complicated as a possible scaffold in organometallic or inorganic system and whose reactivity would diminish compound stability.[1] Studies like that of a 2011 publication on cycloheptatriene double ionization and chemical reactions with xenon present clues for possible reactions with certain conditions and with sulfur involved brings this compound to unmapped territories.[2]
References
[edit]- ^ PubChem. "Cycloheptatriene". pubchem.ncbi.nlm.nih.gov. Retrieved 2025-03-21.
- ^ Ascenzi, Daniela; Aysina, Julia; Zins, Emilie-Laure; Schröder, Detlef; Žabka, Jan; Alcaraz, Christian; Price, Stephen D.; Roithová, Jana (2011-11-07). "Double ionization of cycloheptatriene and the reactions of the resulting C7H(n)2+ dications (n = 6, 8) with xenon". Physical Chemistry Chemical Physics: PCCP. 13 (41): 18330–18338. Bibcode:2011PCCP...1318330A. doi:10.1039/c1cp21634a. ISSN 1463-9084. PMID 21814673.