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Mass spectrometry study of the pyrolysis of perfluoroolefin oxides
Authors:N. D. Kagramanov  A. A. Kutin  N. V. Peschanskii  A. Ya. Zapevalov  L. S. German
Affiliation:(1) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow
Abstract:The pyrolysis of perfluoroolefin oxides has been studied by gas chromatography/mass spectrometry at 400–700°C, in a current of He (1ratio10 dilution, contact time 1 sec). For oxides containing a terminal CF2 group, the sole degradation route is through the elimination of difluorocarbene. Pyrolysis of symmetrical disubstituted oxides results in the elimination of a perfluoroalkylfluorocarbene, which subsequently isomerizes to the corresponding perfluoroolefin. In the pyrolysis of unsymmetric disubstituted oxides the elimination of perfluoroalkylfluorocarbenes occurs by both of the possible routes. Trisubstituted oxides eliminate bis-perfluoroalkylcarbenes. The decomposition of tetrasubstituted oxides proceeds along several directions concurrently.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1497–1502, July, 1991.
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