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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2007 Volume 17, Issue 3, Pages 137–138 (Mi mendc3403)

This article is cited in 4 papers

Distinct reactivities of cis- and trans-RFCF=CFBF2 towards XeF2 and the first synthesis of a [trans-RFCF=CFXe]+ salt

H. J. Frohna, V. V. Bardinb

a Department of Chemistry, Institute of Inorganic Chemistry, University of Duisburg-Essen, Duisburg, Germany
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: The competitive reaction of C4F9CF=CFBF2 (cis : trans = 1.2:1) with XeF2 demonstrated for the first time a remarkably lower reaction rate of the trans isomer with respect to the cis isomer in the xenodeborylation reaction (formation of the [C4F9CF=CFXe]+ cation with a cis : trans ratio of 2.5 to 4:1) and allowed us to develop reaction conditions for the syntheses of [trans-C4F9CF=CFXe]+ salts.

Language: English

DOI: 10.1016/j.mencom.2007.05.001



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