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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 18 (1986), S. 41-47 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction was investigated in the gas phase over the range 80-225°C using the photolysis of heptafluoroisopropyl iodide as the source of radicals. The rate constant, based on the value of 1013.36 cm3 mol-1 s-1 for the recombination of i-C3F7 radicals, is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}{{k_3 } \mathord{\left/ {\vphantom {{k_3 } {{\rm cm}^{\rm 3} }}} \right. \kern-\nulldelimiterspace} {{\rm cm}^{\rm 3} }}{\rm mol}^{ - 1} {\rm s}^{ - 1}) = (13.10 \pm 0.20) - {{(14000 \pm 280)} \mathord{\left/ {\vphantom {{(14000 \pm 280)} \theta }} \right. \kern-\nulldelimiterspace} \theta } $$\end{document} where θ = 2.303 RT/cal mol-1. Arrhenius parameters for chlorine abstraction from CCl4 by CF3, C2F5, n-C3F7, and some hydrogenated radicals are compared.
    Additional Material: 1 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 15 (1983), S. 835-844 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of CF3 radicals with H2O (D2O) has been studied over the range of 533-723 K using the photolysis and the pyrolysis of CF3I as the free radical source. Arrhenius parameters for the reactions \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CF}_3 + {\rm X}_2 {\rm O\buildrel{k_x}\over{\to}CF}_3 {\rm X} + {\rm OX} $$\end{document} where X = H or D, relative to CF3 radical recombination are given by \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} {\rm log}k_{\rm H} /k_c^{1/2} = (5.12 \pm 0.11) - (16,804 \pm 335)/\theta \\ {\rm log}k_{\rm D} /k_c^{1/2} = (5.03 \pm 0.16) - (17,803 \pm 456)/\theta \\ \end{array} $$\end{document} where k/kc1/2 is in cm3/2/mol1/2·s1/2 and θ = 2.303RT/cal/mol. The activation energy and the primary kinetic isotope effect have been compared with those derived from the BEBO method.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 635-642 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relaxation rate constants for the collisional deactivation of I (2P1/2) by halogen cyanides were measured by time resolved atomic absorption. The values obtained were (1.2 ± 0.1) × 10-15, (5.2 ± 0.7) × 10-15, and (2.6 ± 0.4) × 10-14 cm3 molecule-1 s-1 for ClCN, BrCN, and ICN, respectively. Quenching efficiencies are discussed in view of the stability of linear molecules to form the transient complex as well as the similarities assumed between halogen cyanides and interhalogen diatomic molecules.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 1287-1296 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the gas-phase thermal isomerization between trans- and cis-1,2-bis(trifluoromethyl)-1,2,3,3-tetrafluorocyclopropane as well as their decomposition to trans- and cis-perfluoro-2-butene, respectively, and CF2, was studied in the temperature range of 473-533°K, with an initial pressure of reactant of 1.5 to 7.0 Torr. Some runs were also made with the addition of SF6 as an inert gas up to a total pressure of 100 Torr. The reactions are first order and homogeneous. The rate constants for the geometrical isomerization fit the following Arrhenius relations: \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\log {k}_{{trans}\to {cis}}}\mathord{\left/{\vphantom {{\log {k}_{{trans}\to {cis}}}{(\sec ^{ - 1})}}}\right.\kern-\nulldelimiterspace}{(\sec ^{ - 1})}}{ = }{{{(15}{.15}\pm{0}{.16)-(44,487}\pm{ 374)}}\mathord{\left/ {\vphantom {{{(15}{.15} \pm{0}{.16) - (44,487 }\pm { 374)}}{4.576{ }T}}} \right.\kern-\nulldelimiterspace} {4.576{ }T}} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\log {k}_{{trans}\to {cis}}}\mathord{\left/{\vphantom {{\log {k}_{{trans}\to {cis}}}{(\sec ^{ - 1})}}}\right.\kern-\nulldelimiterspace} {(\sec ^{ - 1})}}{ = }{{{(15}{.35} \pm {0}{.19) - (43,419 } \pm { 428)}} \mathord{\left/ {\vphantom {{{(15}{.35} \pm {0}{.19) - (43,419 } \pm { 428)}} {4.576{ }T}}} \right. \kern-\nulldelimiterspace} {4.576{ }T}} $$\end{document} and the corresponding equations for the decomposition of the trans and cis-cyclopropane are \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\log {k}_{{trans}}} \mathord{\left/ {\vphantom {{\log {k}_{{trans}}} {(\sec ^{ - 1})}}} \right. \kern-\nulldelimiterspace} {(\sec ^{ - 1})}}{ = }{{{(15}{.14} \pm {0}{.28) - (46,700} \pm { 652)}} \mathord{\left/ {\vphantom {{{(15}{.14} \pm {0}{.28) - (46,700 } \pm { 652)}} {4.576{ }T}}} \right. \kern-\nulldelimiterspace} {4.576{ }T}} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {{\log {k}_{{cis}}} \mathord{\left/ {\vphantom {{\log {k}_{{cis}} } {(\sec ^{ - 1})}}} \right. \kern-\nulldelimiterspace} {(\sec ^{ - 1})}}{ = }{{{(15}{.39} \pm {0}{.26) - (46,639} \pm { 598)}} \mathord{\left/ {\vphantom {{{(15}{.39} \pm {0}{.26) -(46,639 } \pm { 598)}} {4.576{ }T}}} \right. \kern-\nulldelimiterspace} {4.576{ }T}} $$\end{document}.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 187-196 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of C2F5 radicals with HCN has been studied over the range of 533-673 K using the pyrolysis of pentafluoroethyl iodide as the free-radical source. Arrhenius parameters for the reaction relative to C4F10 recombination are given by \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k_{\rm H} /k_{c^{1/2} } = (5.36 \pm 0.15) - (57.3 \pm 1.8)/\theta $$\end{document} where θ = 2.303RT kJ/mol and kH/kc1/2 is in cm3/2/mol1/2·s1/2.
    Additional Material: 2 Ill.
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