Issue 19, 1976

Polyfluoroallyl cations

Abstract

Polyfluoropropenes (CF3·CF[double bond, length as m-dash]CFX) have been treated with antimony pentafluoride in sulphur dioxide at low temperatures. When X =p-MeO·C6H4, both cis- and trans-isomers gave the same long-lived allyl cation, which was observed by n.m.r. spectroscopy; quenching with methanol gave methyl 2,3-difluoro-3-(p-methoxyphenyl)-acrylate. In the case X = OMe, there is some C-1, C-3 interaction in the observed allyl cation; in the cases X = Ph or Me species were obtained which were not characterised. A long-lived ion was not observed with hexafluoropropene but dimerisation occurred. Cyclobutenium ions have been generated from 1,2-dimethyl- and 1,2-dimethoxy-3,3,4,4-tetrafluorocyclobutenes; these ions have charge concentrated at C-1 and C-3.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 2107-2112

Polyfluoroallyl cations

R. D. Chambers, A. Parkin and R. S. Matthews, J. Chem. Soc., Perkin Trans. 1, 1976, 2107 DOI: 10.1039/P19760002107

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