100758-38-1Relevant articles and documents
Regiospecific fluorination of the aryl group in C6F5I and the preparation of C6F7IF2 - The first perfluorovinyl iodine (III) compound
Frohn,Nielinger
, p. 143 - 146 (1996)
Pentafluoroiodobenzene was oxidized regiospecificly by IF5/BF3 in CH2C12 to 1-iodo-heptafluoro-1,4-cyclohexadiene. With bromo- and chloro-pentafluorobenzene as substrates, the addition of two fluorine atoms to the aromatic ring proceeded analogously but more slowly. 1-Iodo-heptafluoro-1,4-cyclohexadiene was converted to 1-difluoroiodo-heptafluoro-1,4-cyclohexadiene by low-temperature fluorination. The thermal stability and reactivity of the first example of a perfluorinated vinyl iodine(III) compound are reported.
FLUORINATION OF POLYFLUOROAROMATIC COMPOUNDS WITH VANADIUM PENTAFLUORIDE
Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Yakobson, G. G.,Krasilnikov, V. A.,et al.
, p. 37 - 46 (2007/10/02)
Fluorination of polyfluoro-derivatives of benzene and diphenyl with vanadium pentafluoride at -25 to -10 deg C afforded fluorinated cyclohexadienes and cyclohexenes.Octafluoronaphthalene was converted under these conditions to perfluoro-1,4-dihydronaphthalene, perfluorotetralin, perfluoro-1,4,5,8-tetrahydronaphthalene and perfluoro-1,2,3,4,5,8-hexahydronaphthalene.