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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 327-349 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Observations are reported of the effect of the buffer gases He, Ne, and CF4, in the pressure range of 0-30 torr, on the branching ratio [HCl]/[DCl] of the unimolecular decomposition The ratio R = kH/kD has been measured in high-pressure thermal decomposition (670-1100 K) and was shown to give a unique measure of the internal energy of the decomposing molecules and hence, with RRKM theory and pressure fall-off data, a time scale for their decomposition.Applying the thermal data to the photolysis leads to the conclusion that excitation and decomposition are produced by the laser spike (high intensity, 70 ns FWHM) and also at a slower rate by the larger, less intense tail (1.6 μs). Added buffer gases quench the latter, leaving the former which, from measurements of R, is shown to correspond to excitations of 115 ± 15 kcal/mol and lifetimes of ∼30 ps. No bond breaking is seen despite the high energies, in accord with theoretical expectations. The results require an enhanced rate of photon absorption by the highly excited molecules, which are about hundredfold greater than that observed for 300 K molecules. Data are also reported for C2H2F2 and the secondary multiphoton photolysis of the ethylenes produced. Effects of beam geometry and wavelength are explored.
    Additional Material: 12 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. 1235-1236 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 77-90 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanisms for the conversion of molecular tritium gas to tritiated water are examined for tritium mixtures with (1) oxygen and nitrogen, (2) oxygen and argon, and (3) water and helium, for which previous experimental data exist. By analyzing results of these experiments in light of the radiation chemistry involved in a mixture of tritium and other gases, an understanding of the conversion mechanisms is reached. The formation of H and/or OH free radicals as intermediate species is of particular significance in the formation of HTO in that these radicals initiate a number of reactions which lead to the formation of water. These reactions are analyzed in terms of steady-state kinetics to obtain predictive models which can be judged against the experimental observations. For the three experimentally observed mixtures, model agreement is found to be within a factor of 2-3.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 63-75 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of deuterated ethyl chloride CH2DCH2Cl was studied in a static system in the pressure range of 0.1-26 torr, and the Arrhenius expression for the overall decomposition at the high-pressure limit and in the temperature range of 670-1100 K was found to be \documentclass{article}\pagestyle{empty}\begin{document}$$ k_\infty = 10^{13.33 \pm 0.10} \exp [(- 57,200 \pm 500){\rm cal/mol/}RT]{\rm}s^{- 1} $$\end{document}The intramolecular isotopic effects were first examined in the pressure range of 0.1-26 torr at 837 K, and the branching ratio kH/kD was found to decrease with increasing pressure. The RRKM-theory calculations describe the experimental data well.The intramolecular isotopic effect was also examined in the temperature range of 728-926 K, and the branching ratio at the high pressure limit was given by the expression \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{\rm H} /k_{\rm D} = (1.44 \pm 0.05)\exp [(1500 \pm 50){\rm cal/mol/}RT] $$\end{document} when kH and kD are the rate constants for the HCl and DCl channels of elimination.The Arrhenius A factors obtained at the high-pressure limit together with the temperature-dependent expression of the branching ratio provided additional experimental data for an assignment (fine-tuned) of the vibrational frequencies of both activated complexes involved in the thermal decomposition of CH2DCH2Cl. The evaluated vibrational frequencies were then used in the RRKM calculations describing the pressure dependence of the intramolecular isotopic effect. The RRKM calculations and the experimental data were in good agreement, supporting the choice of vibrational frequencies for both the activated complexes as well as the transition-state model.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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