Chemical compound
Fluorocyclopropane is an organofluorine compound with the chemical formula C3 H5 F . The compound is a member of haloalkane family.[ 1]
Synthesis
The compound can be produced by reacting imidazolylidene cyclopropyl group with xenon difluoride .[ 2]
Also, a reaction of enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids .[ 3]
See also
References
^ Kerr, J. A.; Kirk, A. W.; O'Grady, B. V.; Phillips, D. C.; Trotman-Dickenson, A. F. (1967). "Kinetics of decomposition of chemically activated alkyl fluorides" . Discussions of the Faraday Society . 44 : 263. doi :10.1039/DF9674400263 . Retrieved 29 May 2023 .
^ Mankad, Neal P.; Toste, F. Dean (2012). "C(sp 3 )–F reductive elimination from alkylgold( iii ) fluoride complexes" . Chem. Sci. 3 (1): 72– 76. doi :10.1039/C1SC00515D . PMC 3474378 . Retrieved 29 May 2023 .
^ Delion, Laëtitia; Poisson, Thomas; Jubault, Philippe; Pannecoucke, Xavier; Charette, André B. (September 2020). "Synthesis of fluorocyclopropanes via the enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids" . Canadian Journal of Chemistry . 98 (9): 516– 523. doi :10.1139/cjc-2020-0036 . ISSN 0008-4042 . Retrieved 29 May 2023 .
Dall'O, L.; Heydtmann, H. (January 1987). "Kinetic Study of Chemically Activated Fluorocyclopropane". Berichte der Bunsengesellschaft für physikalische Chemie . 91 (1): 24– 30. doi :10.1002/bbpc.19870910107 .
Casas, F.; Kerr, J. A.; Trotman-Dickenson, A. F. (1964). "706. Fluorinated cyclopropanes. Part II. The thermal isomerization of monofluorocyclopropane". Journal of the Chemical Society (Resumed) : 3655. doi :10.1039/JR9640003655 .
Salts and covalent derivatives of the
fluoride ion
PF− 6 , AsF− 6 , SbF− 6 compoundsAlF2− 5 , AlF3− 6 compoundschlorides, bromides, iodides and pseudohalogenides SiF2− 6 , GeF2− 6 compoundsOxyfluorides Organofluorides with transition metal, lanthanide, actinide, ammonium nitric acids bifluorides thionyl, phosphoryl, and iodosyl