Free Radical Addition to Olefins: Part 11.—Telomerization of Tetrafluoroethylene with Dibromodifluoromethane and Trifluoroiodomethane

dc.contributor.authorAshton, David S.
dc.contributor.authorTedder, John M.
dc.contributor.authorWalton, John C.
dc.date.accessioned2025-06-23T11:17:37Z
dc.date.available2025-06-23T11:17:37Z
dc.date.issued1974
dc.description.abstractThe telomerization of tetrafluoroethylene in the gas phase by CF2Br2 results in the formation of products of general formula Br[CF2]„Br n = 2-11. When CF3I was used the products were found to be CF3[CF2CF2]„I where n = 1 to 5. Transfer constants have been determined for radicals con taining various numbers of tetrafluoroethylene units, and Arrhenius parameters from temperature variation data. Trends in the transfer constants are compared with previous work in solution. The activation energies from the transfer constants are combined with known values of the activation energies of the addition steps to give estimates of the activation energies of the halogen abstraction steps.en_US
dc.identifier.urihttps://dspace.bits-pilani.ac.in/handle/123456789/18974
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (1-6)en_US
dc.subjectChemistryen_US
dc.subjectFree Radicalen_US
dc.subjectOlefinsen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleFree Radical Addition to Olefins: Part 11.—Telomerization of Tetrafluoroethylene with Dibromodifluoromethane and Trifluoroiodomethaneen_US
dc.typeArticleen_US

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