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Polar addition of perfluoro-tert-hexyl iodide to alkenes and alkynes
Authors:S. I. Pletnev  S. M. Igumnov  I. N. Rozhkov  G. D. Rempel'  V. I. Ponomarev  L. E. Deev  V. S. Shaidurov
Affiliation:(1) A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow
Abstract:The effective charges on the atoms in molecules of perfluoroalkyl halides of general formula (CF3)nCF3–nX (X=Cl, Br, I) have been calculated by the AM1 semiempirical method. In polar solvents perfluoro-tert-hexyl iodide is reduced under the action of alkenes and aromatic hydrocarbons to form 2-hydroperfluoro-2-methyl-pentane and perfluoro-2-methyl-2-pentene. In ethyl acetate the regio- and stereo-specific addition of perfluoro-tert-hexyl iodide to alkenes, butadiene, and alkynes takes place, which is associated with the realization of a polar ion-radical mechanism for the reaction.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2057–2061, September, 1989.
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