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

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dc.contributor.author Ashton, David S.
dc.contributor.author Tedder, John M.
dc.contributor.author Walton, John C.
dc.date.accessioned 2025-06-23T11:17:37Z
dc.date.available 2025-06-23T11:17:37Z
dc.date.issued 1974
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18974
dc.description.abstract The 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.language.iso en en_US
dc.publisher Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (1-6) en_US
dc.subject Chemistry en_US
dc.subject Free Radical en_US
dc.subject Olefins en_US
dc.subject Journal of the Chemical Society : Faraday Transaction - I en_US
dc.title Free Radical Addition to Olefins: Part 11.—Telomerization of Tetrafluoroethylene with Dibromodifluoromethane and Trifluoroiodomethane en_US
dc.type Article en_US


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