Fluoromethylidyne
From Wikipedia, the free encyclopedia
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IUPAC name
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3D model (JSmol) |
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CompTox Dashboard (EPA) |
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| CF• | |||
| Molar mass | 31.0091 g mol−1 | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Fluoromethylidyne is not a stable chemical species but a metastable radical containing one highly reactive carbon atom bound to one fluorine atom with the formula CF.[1] The carbon atom has a lone-pair and a single unpaired (radical) electron in the ground state.[2]
Ground-state fluoromethylidyne radicals can be produced by the ultraviolet photodissociation of dibromodifluoromethane at 248 nanometer wavelength.[3]
It readily and irreversibly dimerises to difluoroacetylene, also known as difluoroethyne, perfluoroacetylene, or di- or perfluoroethylyne. Under certain conditions it can hexamerise to hexafluorobenzene.

