1982
DOI: 10.1039/f19827803493
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Reaction of pentafluoroethyl radicals with cyanogen chloride

Abstract: The reaction of C,F, radicals with cyanogen chloride was studied between 293 and 573 K, using perfluoroethyl iodide as the free-radical source. CJ,. The reactions involved areThe main product, C2F,C1, is tormed via an addition reaction or

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Cited by 4 publications
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“…and R the rate of formation. If the mechanism is accepted and the formation of CF3H through reaction ( 5 ) is not important at low conversion, a is related to the measured ratio [CF3CN]/[CF3H] and could be estimated as (RCF3CN/RCF3W) -1.…”
Section: Resultsmentioning
confidence: 99%
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“…and R the rate of formation. If the mechanism is accepted and the formation of CF3H through reaction ( 5 ) is not important at low conversion, a is related to the measured ratio [CF3CN]/[CF3H] and could be estimated as (RCF3CN/RCF3W) -1.…”
Section: Resultsmentioning
confidence: 99%
“…Similar behaviour was observed for the reactions of C2F5, n-C3F7 and i-C3F7 with C1CN. [5][6][7] We now present results for the reaction of CF3 radicals generated by photolysis of CF,I with HCN in the temperature range 333-523 K.…”
mentioning
confidence: 99%