Aa. Pud et al., CATHODIC TRANSFORMATIONS OF PERFLUORO-2,4-DIMETHYL-3-ETHYLPENTANE ANDITS UNSATURATED ANALOGS, Russian journal of electrochemistry, 32(3), 1996, pp. 337-342
Electrochemical reduction of perfluoro-2,4-dimethyl-3-ethylpentane (C9
F20) and its unsaturated analogs, i.e., the perfluoro-2,4-dimethyl-3-e
thyl-3-pentyl (C9F19) stable radical and a mixture of isomeric trimers
of hexafluoropropylene (C9F18), is studied. It is shown that the redu
ction of C9F20 is a multistep process, is accompanied by a cleavage of
the C-F bond, and occurs via formation of C9F19, C9F18, and other int
ermediates of the carbanion nature.