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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 361-367 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: CF3 radicals were generated by the photolysis of perfluoroacetic anhydride. In the presence of pentafluorobenzene, the CF3 radicals react according to the following mechanism: It was found that the addition reaction (3) becomes reversible above ca. 453 K. The addition rate parameters have been revised and they satisfactorily agree with those reported previously.At temperatures higher than 593 K, only true H-abstraction occurs. The rate constant kH for reaction (5) is given by: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log [(k_{\rm H} /k_c^{1/2}){\rm mol}^{- 1/2} \,{\rm cm}^{{\rm 3/2}} \,{\rm s}^{{\rm - 1/2}}]\, = \,(4.34\, \pm \,0.43)\, - \,(59,00\, \pm \,2.62)/\theta $$\end{document} where θ = 2.303 RT kJmol-1 and kc is the rate constant for combination of CF3 radicals. The reactions of CF3 with benzene and pentafluorobenzene are compared.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1357-1370 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase reaction of CF3 with HCN has been examined over a wide conversion range using CF3I as a thermal and photolytic source of radicals. Quantitative and qualitative results show a significant increase of the specific rate constant for the hydrogen abstraction reaction relative to CF3 recombination when reaction is carried out under ultraviolet irradiation. This “extra” formation of the reaction product, CF3H, has been assigned to the participation of iodine in this system through the formation of a (I-HCN) intermediate. Arrhenius parameters obtained for the addition mechanism of I to HCN do not seem to conform to a single reaction step, on the contrary, they correspond to a more complex reaction scheme.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 47-56 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolysis of C2F5I with CF3COOH in the temperature range 473-533 K was studied in the gas phase.Evidence is presented that supports a complex mechanism for the formation of C2F5H through the H-atom abstraction reaction from CF3COOH by C2F5 radicals as well as the participation of I(2P½).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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