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Chlorosyl fluoride

From Wikipedia, the free encyclopedia
Chlorosyl fluoride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/ClFO/c2-1-3
    Key: AXCBHWGTRNNXKG-UHFFFAOYSA-N
  • O=ClF
Properties
ClFO
Molar mass 70.45 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Chlorosyl fluoride is an inorganic compound of chlorine, fluorine, and oxygen with the chemical formula OClF.[1] [2] [3]

Synthesis

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Chemical properties

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Chlorosyl fluoride is thermolabile and disproportionates to ClF and ClO
2
F
.:[4]

2FClO → ClF + FClO2
2FClO → 2ClF +O2

References

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  1. ^ Müller, Holger S. P (10 December 1999). "Infrared spectroscopy and molecular properties of chlorosyl fluoride, FClO". Chemical Physics Letters . 314 (5): 396–402. Bibcode:1999CPL...314..396M. doi:10.1016/S0009-2614(99)01197-5. ISSN 0009-2614.
  2. ^ Müller, Holger S. P.; Cohen, Edward A. (8 February 2002). "The molecular properties of chlorosyl fluoride, FClO, as determined from the ground-state rotational spectrum". The Journal of Chemical Physics . 116 (6): 2407–2416. Bibcode:2002JChPh.116.2407M. doi:10.1063/1.1433002. ISSN 0021-9606.
  3. ^ Vogt, J. (2011). "755 ClFO Chlorosyl fluoride". Asymmetric Top Molecules. Part 3. Landolt-Börnstein - Group II Molecules and Radicals. 29D3. Springer Berlin Heidelberg: 296–298. Bibcode:2011LanB.29D3..296V. doi:10.1007/978-3-642-14145-4_177. ISBN 978-3-642-14144-7.
  4. ^ a b c Haupt, Axel (22 March 2021). Organic and Inorganic Fluorine Chemistry: Methods and Applications. Walter de Gruyter GmbH & Co KG. p. 139. ISBN 978-3-11-065933-7 . Retrieved 27 March 2023.
Salts and covalent derivatives of the fluoride ion
HF ?HeF2
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
PF6, AsF6, SbF6 compounds
AlF2−5, AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl

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