Stibole is a theoretical heterocyclic organic compound, a five-membered ring with the formula C4H4SbH. It is classified as a metallole. It can be viewed as a structural analogofpyrrole, with antimony replacing the nitrogen atom of pyrrole. Substituted derivatives, which have been synthesized, are called stiboles.
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| Names | |||
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| Preferred IUPAC name
1H-Stibole | |||
| Identifiers | |||
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3D model (JSmol) |
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| ChemSpider | |||
PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |||
| C4H5Sb | |||
| Molar mass | 174.844 g·mol−1 | ||
| Related compounds | |||
Related compounds |
Pyrrole, phosphole, arsole, bismole | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2,5-Dimethyl-1-phenyl-1H-stibole, for example, can be formed by the reaction of 1,1-dibutyl-2,5-dimethylstannole and dichlorophenylstibine.[1] Stiboles can be used to form ferrocene-like sandwich compounds.[2]
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