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  • Physical Chemistry  (258)
  • Wiley-Blackwell  (258)
  • Annual Reviews
  • Oxford University Press
  • Periodicals Archive Online (PAO)
  • 1980-1984  (258)
  • 1935-1939
  • 1984  (135)
  • 1981  (123)
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  • Wiley-Blackwell  (258)
  • Annual Reviews
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  • 1980-1984  (258)
  • 1935-1939
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  • 101
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 119-123 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactivity of amines towards tert-butoxy radicals depends upon the amine ionization potential and the solvent, indicating that polar structures contribute to the reactivity of these compounds. Nevertheless, the dependence with the amine potential is smaller than the one obtained for the quenching of carbonyl excited states by amines and other factors as the strength of the broken hydrogen bond and steric hindrance are also significant in determining the rate of the process.
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  • 102
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 741-753 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the thermal decomposition of an acetylene-ethane-d6 mixture indicates that the rate constant for hydrogen abstraction from acetylene by methyl is more than 20 times less than for abstraction from ethane. Isotopic exchange is initiated by a rapid reaction between product D atoms and C2H2. A series of experiments involving the reactions of a D2-acetylene mixture indicated that a molecular exchange process was also occurring, and it was shown that d[C2HD]/dt = k[D2]0.7[C2H2]0.3, effective activation energy = 15.8 kcal/mol. This mechanism made an insignificant contribution to isotope exchange in C2H2-C2D6 mixtures.
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  • 103
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 817-831 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methyl nitrate decomposition is accompanied by self-heating. Using very fine thermocouples, direct measurements of excess temperatures have been made to establish the intensity and extent of self-heating in nonisothermal reaction. The measurements are displayed as contourlines of equal degrees of temperature excess on the pressure-temperature ignition diagram.A twofold kinetic investigation has been made of the overall reaction. One part concentrates on achieving isothermal conditions and full characterization of intermediate products. It uses mass-spectrometric analyses both to establish stoichiometry throughout decomposition and to validate velocity constant measurements derived from continuous pressure-time records. The best value for E = 151 ± 3 kJ/mol is about 10 kJ/mol less than previously.The other part deliberately invades the nonisothermal region to test the qualitative and quantitative predictions of theory (1) that uncorrected reaction orders and activation energies will exceed their isothermal values, (2) that their relative excess (δn/n, δE/E) will be about the same, and (3) that they will be dependent in a simple and predictable way on the reduced excess central temperature.
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  • 104
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 785-786 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 105
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 787-788 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 106
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 833-844 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arrhenius parameters for the decomposition reactions of various alkoxy radicals are evaluated. The recommended values for tert-butoxy radical decomposition reaction are log A (s-1) = 14.1, Ea = 15.3 kcal/mol. The parameters give reasonably self-consistent results with related rate constants, product distributions of hydrocarbon oxidation reactions, and the values reported in different laboratories in different environments.A reworking of data by Batt et al. on RO + NO and RO + NO2 leads to a lowering of his A factors for these reactions by a factor of 5. It also leads to a similar lowering of the A factors for RO decompositions. The intrinsic activation energies E for the addition of alkyl radicals R to the carbonyl group are not only found to be a function of the exothermicity of reaction, but they are also dependent on the nucleophilicity of the alkyl radicals. For each radical R (Me, Et, i-Pr) the data can be fit to an Evans-Polanyi plot E = a + b (δH), where a uniform slope b = 0.58 can be found for all R. The intercepts a are then found to decrease nearly linearly with the decreasing ionization potential of R, namely, a = 2.1 [IP] - 6.2 (kcal/mol), with the ionization potential given in electron volts.
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  • 107
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 108
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 7-21 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase decompositions of methylsilane and methylsilane-d3 have been investigated in a single-pulse shock tube at 4700 torr total pressure in the temperature range of 1125-1250 K. For CH3SiD3 at 1200 K three primary steps occur in the homogeneous decomposition with efficiencies in parentheses: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm SiD}_{\rm 3} \mathop {\longrightarrow} \limits^1 {\rm CH}_{\rm 3} {\rm SiD} + {\rm D}_{\rm 2} \left( {0.71} \right) $$\end{document}, \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm SiD}_{\rm 3} \mathop {\longrightarrow} \limits^2 {\rm CH}_{\rm 4} + {\rm SiD}_{\rm 2} \left( {0.15} \right) $$\end{document}, and \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm SiD}_{\rm 3} \mathop {\longrightarrow} \limits^3 {\rm CH}_{\rm 2} \raise1pt\hbox{=\kern-3.45 pt=} {\rm SiD}_{\rm 2} \left( {0.14} \right) $$\end{document}. For CH3SiH3 at 1200 K the primary CH4 elimination efficiency is 0.09 while the total primary H2 elimination efficiency is 0.91. Minor product formations of C2H4, acetylene, dimethylsilane, and SiH4 are discussed.
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  • 109
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    International Journal of Chemical Kinetics 16 (1984), S. 41-55 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constants for the reactions of OH + HO2NO2 (1) and OH + HNO3 (2) have been measured with the technique of flash photolysis resonance fluorescence over the temperature ranges of 240-330 K at 760 torr He for reaction (1) and of 240-370 K at 50 and 760 torr He for reaction (2). Reactant concentrations were monitored continuously by ultraviolet and infrared spectrophotometry. The data can be fitted to the following Arrhenius expressions: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = \left( {5.9 \pm 0.4} \right) \times 10^{ - 13} \exp \left[ {{{\left( {650 \pm 30} \right)} \mathord{\left/ {\vphantom {{\left( {650 \pm 30} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right]{{{\rm cm}^{\rm 3} } \mathord{\left/ {\vphantom {{{\rm cm}^{\rm 3} } {{\rm molecule} \cdot {\rm s}}}} \right. \kern-\nulldelimiterspace} {{\rm molecule} \cdot {\rm s}}} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm SiD}_{\rm 3} \mathop {\longrightarrow} \limits^3 {\rm CH}_{\rm 2} \raise1pt\hbox{=\kern-3.45 pt=} {\rm SiD}_{\rm 2} \left( {0.14} \right) $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_2 = \left( {8.3 \pm 0.9} \right) \times 10^{ - 15} \exp \left[ {{{\left( {850 \pm 40} \right)} \mathord{\left/ {\vphantom {{\left( {850 \pm 40} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right]{{{\rm cm}^{\rm 3} } \mathord{\left/ {\vphantom {{{\rm cm}^{\rm 3} } {{\rm molecule} \cdot {\rm s}}}} \right. \kern-\nulldelimiterspace} {{\rm molecule} \cdot {\rm s}}} $$\end{document} These results are in very good agreement with recent studies of reaction (2), and also of reaction (1) at 295 K.
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  • 110
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 57-67 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficients for the gas-phase pyrolyses of a series of structurally related secondary acetates have been measured in a static system over the temperature range of 289.1-359.5°C and the pressure range 50.0-203.0 torr. The temperature dependence of the rate coefficients is given by the following Arrhenius equations: for 3-hexyl acetate, log k1 (s-) = (12.12 ± 0.33) - (176.1 ± 3.9)kJ/mol/2.203RT; for 5-methyl-3-hexyl acetate, log k1 (s-) = (13.17 ± 0.20) - (186.2 ± 2.3)kJ/mol/2.303RT; and for 5,5-dimethyl-3-hexyl acetate, log k1 (s-) = (12.70 ± 0.19) - (177.4 ± 2.2)kJ/mol/2.303RT. The direction of elimination of these esters has shown from the invariability of olefin distributions at different temperatures and percentages of decomposition that steric hindrance is a determining factor in the eclipsed cis conformation. Moreover, a more detailed analysis indicates that the greater the alkyl-alkyl interaction, the less favored the elimination tends to be. Otherwise, an increase of alkyl-hydrogen interaction caused steric acceleration to be the determining factor.
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  • 111
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    International Journal of Chemical Kinetics 16 (1984), S. 103-115 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the thermal reaction between CF3OF and C3F6 have been investigated between 20 and 75°C. It is a homogeneous chain reaction of moderate length where the main product is a mixture of the two isomers 1-C3F7OCF3 (68%) and 2-C3F7OCF3 (32%). Equimolecular amounts of CF3OOF3 and C6F14 are formed in much smaller quantities. Inert gases and the reaction products have no influence on the reaction, whereas only small amounts of oxygen change the course of reaction and larger amounts produce explosions.The rate of reaction can be represented by eq. (I): The following mechanism explains the experimental results: Reaction (5) can be replaced by reactions (5a) and (5b), without changing the result: Reaction (4) is possibly a two-step reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ E_1 = 15.90 \pm 0.45{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = \left( {7.60 \pm 0.68} \right)10^8 {\rm exp}\left( { - 15,900\,\, \pm \,\,450\,\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \cdot s^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ E^ * \, = \,12.30\, \pm \,0.25\,{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k^ * \, = \,\left( {6.11\, \pm \,0342} \right)10^7 \,{\rm exp}\left( { - 12,300\, \pm \,250\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \, \cdot \,{\rm s}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {E^ * \, - \frac{1}{2}E_1 \, = \,4.35\,{\rm kcal}\, = \,E_3 \, - \,\frac{1}{2}E_4 ;} & {E_3 \,} \\ \end{array} 〉 \,4.35\,{\rm kcal} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \nu \,\left( {{\rm chain}\,{\rm length}} \right)\, = \,1 + \,\frac{{k_3 }}{{k_1 ^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} \left( {2k_4 } \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} }}\left( {\frac{{\left| {{\rm CR}_{\rm 3} {\rm OF}} \right|}}{{\left| {{\rm C}_{\rm 3} {\rm F}_{\rm 6} } \right|}}} \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} $$\end{document} For ∣CF3 = ∣C3F6∣, ν20°C = 36.8, ν50°C = 24.0, and ν70°C = 14.2.
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  • 112
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    International Journal of Chemical Kinetics 16 (1984), S. 159-193 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new reaction mechanism describing the atmospheric photochemical oxidation of toluene is formulated and tested against environmental chamber data from the University of California, Riverside, Statewide Air Pollution Research Center (SAPRC). On simulations of toluene - NOx and toluene - benzaldehyde - NOx irradiations, the average predicted O3 and PAN maxima are within 3% of the experimental values. Simulations performed with the new mechanism are used to investigate various mechanistic paths, and to gain insight into areas where our understanding is not complete. Specific areas that are investigated include benzaldehyde photolysis, organic nitrate formation, alternate ring fragmentation pathways, and conjugated γ-dicarbonyl condensation to the aerosol phase.
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  • 113
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    International Journal of Chemical Kinetics 16 (1984), S. 221-230 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the reactions of iron(III) with diglycolic, tartaric, and citric acids have been studied in aqueous acid solutions by the temperature-jump method at 25.0°C and at ionic strengths 1.0 (for tartaric and citric acids) and 0.50 mol/dm3 (for diglycolic acid). The experimental data indicate that iron(III) monochelate formation occurs by the same reaction mechanism for all three ligands examined and that only pathways involving the FeOH2+ ion contribute to the chelation process. The reacting species for citric acid is the undissociated ligand. For tartaric and diglycolic acids both the neutral ligands and the corresponding monoanions react significantly under the experimental conditions used. Kinetic evidence for the contribution of intermediate steps to the limiting rate in the overall chelate-formation process has been obtained and discussed.
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  • 114
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    International Journal of Chemical Kinetics 16 (1984), S. 31-39 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The homogeneous gas-phase decomposition kinetics of methylsilane and methylsilane-d3 have been investigated by the comparative-rate-single-pulse shock-tube technique at total pressures of 4700 torr in the 1125-1250 K temperature range. Three primary processes occur: CH3SiH3 → CH3SiH + H2 (1), CH3SiH3 → CH4 + SiH2 (2), and CH3SiH3 → CH2 = SiH2 + H2 (3). The high-pressure rate constants for the primary processes in CH3SiH3 obtained by RRKM calculations are log (k1 + k3) (s-1) = 15.2 - 64,780 Cal/θ and log k2 (s-) = 14.50 - 67,600 → 2800 Cal/θ. For CH3SiD3 these same rate constants are log k1 (s-) = 14.99 - 64,700 cal/θ log k2 (s-) = 14.68 - 66,700 → 2000 cal/θ, and log k3 (s-) = 14.3 - 64,700 cal/θ.
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  • 115
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    International Journal of Chemical Kinetics 16 (1984) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 116
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    International Journal of Chemical Kinetics 16 (1984), S. 23-30 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The static system pyrolysis of methylsilane (T ∼ 700 K, PT ∼ 150 torr), pure and in the presence of ethylene, propylene, and acetylene, has been investigated. It is proposed that in the uninhibited system, the major products (silane and dimethylsilane) are produced by free radical processes, and that the free radicals are formed at the walls from methylsilylenes. In the presence of olefins, the free radicals are trapped to form methylsilane adducts. In acetylene, trapping of methylsilylenes prevents free radical production and eliminates the free radical produced products of the pure and the olefin inhibited systems. Rates of initiation correlate with rates of reactant loss in acetylene inhibited systems, and with rates of hydrogen formation in olefin inhibited systems. Rough estimates of primary dissociation process yields give for the 1,1-H2 elimination φ1,1 ≅ 0.78, for the 1,2-H elimination φ1,2 ≅ 0.16, and for the methane elimination φCH4 ≅ 0.06 at 700 K. Deuteration lowers initial step kinetics by about 15%.
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  • 117
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cross-disproportionation/combination ratios for CFH2 and CF3 with C2H5 radicals have been determined to be Δ = 0.032 ± 0.012 and δ = 0.098 ± 0.020, respectively, over the temperature range 25-75°C. For the pathway that yields CFH and C2H6, δ = 0.020 ± 0.005 at 25°C.
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  • 118
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    International Journal of Chemical Kinetics 16 (1984), S. 117-124 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The static vessel pyrolysis of bicyclo[2.2.2]octa-2,5,7-triene (barrelene) has been studied between 483 and 523 K. The products were acetylene and benzene (in equal quantities) with no other detectable C8H8 isomer (down to less than 1% of total). The time dependence fitted first-order kinetics, and the data are consistent with a homogeneous unimolecular reaction close to, if not at, its high-pressure limit at 0.25 torr. The rate constant was fitted to the Arrhenius equation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \left( {{k \mathord{\left/ {\vphantom {k {s^{ - 1} }}} \right. \kern-\nulldelimiterspace} {s^{ - 1} }}} \right)\, = \,\left( {14.27\, \pm \,0.18} \right)\, - \,{{\left( {41.71\, \pm \,0.41\,{{{\rm kcal}} \mathord{\left/ {\vphantom {{{\rm kcal}} {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}} \right)} \mathord{\left/ {\vphantom {{\left( {41.71\, \pm \,0.41\,{{{\rm kcal}} \mathord{\left/ {\vphantom {{{\rm kcal}} {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}} \right)} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}\,\ln \,10 $$\end{document} These Arrhenius parameters are shown to imply a concerted single-step process. Alternative mechanisms are discussed and a comparison is made with the retro-Diels - Alder reactions of other bicyclo[2.2.2]octa-olefin systems.
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  • 119
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    International Journal of Chemical Kinetics 16 (1984) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 120
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    International Journal of Chemical Kinetics 16 (1984), S. 195-204 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the oxidation of cyclopentanol, cyclohexanol, 2—methylcyclohexanol, and cycloheptanol by hexacyanoferrate(III) ions in mild alkaline medium has been studied in the presence of traces of ruthenium(VI) ≈ 10-7M at constant ionic strength (0.26M). The results suggest that the oxidation of the studied cyclic alcohols proceeds via the formation of a complex between Ru(VI) and the substrate which slowly decomposes, giving the reduced form of ruthenium which was reoxidized to Ru(VI) in a fast step by alkaline hexacyanoferrate(III) ions. The product study shows the production of the corresponding ketone.
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  • 121
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    International Journal of Chemical Kinetics 16 (1984), S. 205-211 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants for the quenching of O2(1Δg) with carbon disulfide, dimethyl sulfide, dimethyl disulfide, diallyl disulfide, ethyl mercaptan, and thiophene have been determined in a discharge flow system in the absence of oxygen atoms. The rate constants are found to be (6.5 ± 0.6) × 104, (1.8 ± 0.2) × 104, and (3.5 ± 0.6) × 103 L/mol · s for dimethyl sulfide, ethyl mercaptan, and thiophene, respectively. The other compounds have rate constants 〈9.9 × 102 L/mol · s. In the case of dimethyl sulfide, even when NO2 concentration is more than what is required to remove oxygen atoms completely, the rate constants are found to vary with different amounts of NO2. No correlation is found to exist between the logarithm of the rate constants and the ionization potentials of the compounds.
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  • 122
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    International Journal of Chemical Kinetics 16 (1984), S. 251-258 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of the reaction of aqueous sulfite with the N-chloropeptide N-chloroalanylalanylalanine has been studied as a function of pH, temperature, and ionic strength. The results of this work suggest that the mechanism of the reaction involves the interaction of the neutral chloramine with the three ionic forms of sulfite, SO3-2, HSO3-, and H2SO3, with the rate of reaction increasing rapidly with increasing protonation. The estimated second-order rate constants for each ionic species as a function of temperature are \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm H}_{\rm 2} {\rm SO}_{\rm 3} } \hfill & {k_1 \, = \,2.00\, \times \,10^8 \,{\rm exp}\left( {{{ - 1544} \mathord{\left/ {\vphantom {{ - 1544} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right){\rm min}^{ - 1} } \hfill \\ {{\rm HSO}_{\rm 3}^ - } \hfill & {k_2 \, = \,4.35\, \times \,10^4 \,{\rm exp}\left( {{{ - 1170} \mathord{\left/ {\vphantom {{ - 1170} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right){\rm min}^{ - 1} } \hfill \\ {\,\,{\rm SO}_{\rm 3}^{ - 2} } \hfill & {k_3 \, = 1.58\, \times \,10^{12} \,{\rm exp}\left( {{{ - 12,660} \mathord{\left/ {\vphantom {{ - 12,660} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right){\rm min}^{ - 1} } \hfill \\ \end{array} $$\end{document} where the activation energies are in units of cal/mol.
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  • 123
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    International Journal of Chemical Kinetics 16 (1984) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
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  • 124
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    International Journal of Chemical Kinetics 16 (1984), S. 345-352 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochlorination of tetrachloroethylene has been studied in a homogeneous liquid system. Kinetic parameters such as reaction orders for chlorine, tetracholoroethylene and light intensity, preexponential factor, and activation energy were evaluated from experimental data. The following kinetic equation was obtained by parameter estimation following the Marquardt procedure: \documentclass{article}\pagestyle{empty}\begin{document}$$ r = \left( {4.02 \pm 0.46} \right)10^{ - 5} \exp \left( { - \frac{{54,700 \pm 200}}{{RT}}} \right)I^{0.489 \pm 0.003} C_{Cl_2 }^{0.889 \pm 0.160} C_{C_2 Cl_4 }^{1.040 \pm 0.042} $$\end{document}
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  • 125
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    International Journal of Chemical Kinetics 16 (1984), S. 353-369 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction chemistry of C2N2—Ar and C2N2—NO—Ar mixtures has been investigated behind incident shock waves. Progress of the reaction was monitored by observing the cyano radical (CN) in absorption at 388.3 nm. A quantitative spectroscopic model was used to determine concentration histories of CN. From initial slopes of CN concentration during cyanogen pyrolysis, the rate constant for C2N2 + M → 2CN + M (1) was determined to be k1 = (4.11 ± 1.8) × 1016 exp(-47,070 ± 1400/T) cm3/mol · s. A reaction sequence for the C2N2—NO system was developed, and CN profiles were computed. By comparison with experimental CN profiles the rate constant for the reaction CN + NO → NCO + N (3) was determined to be k3 = 10(14.0 ± 0.3) exp(-21,190 ± 1500/T) cm3/mol · s. In addition, the rate of the four-centered reaction CN + NO → N2 + CO (2) was estimated to be approximately three orders of magnitude below collision frequency.
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  • 126
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    International Journal of Chemical Kinetics 16 (1984), S. 371-377 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of tert-butoxyl radicals with amines, leading to the formation of α-aminoalkyl radicals, and the reactions of these with the electron acceptor methyl viologen have been examined using laser flash photolysis techniques. For example, the radicals CH3ĊHNEt2 and HOCH2ĊH N(CH2CH2OH)2 react with methyl viologen with rate constants equal to (1.3 ± 0.1) × 109 and (2.1 ± 0.4) × 109M-1 · s-1, respectively, in wet acetonitrile at 300 K.
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  • 127
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    International Journal of Chemical Kinetics 16 (1984), S. 407-421 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The general effect of back energy transfer is to reduce the apparent quenching constant which is an important parameter in the interpretation of energy transfer data. However, this interpretation may be erroneous when possible diffusion effects and the existence of nonuniform configurational distributions are not taken into account.
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  • 128
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    International Journal of Chemical Kinetics 16 (1984), S. 445-467 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diode laser spectroscopy has been employed to monitor the formation of chlorine nitrate (ClONO2) in the association reaction of ClO with NO2. Chlorine nitrate is the only stable end-product of this reaction at room temperature. Time-resolved measurements of ClONO2 formation using molecular modulation showed no evidence for any involvement of unstable isomers of ClNO3 in the reaction. These measurements gave a value of k1 = (1.8 ± 0.4) × 10-31 cm6/molecule2 · s for the reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm ClO}\,\, + \,\,{\rm NO}_{\rm 2} \,\, + \,\,{\rm M}\mathop {\longrightarrow} \limits^{k_1 } {\rm ClONO}_{\rm 2} \,\, + \,\,{\rm M} $$\end{document} at 295 K and an upper limit of 5 ms for the lifetime of any isomeric products at this temperature.
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  • 129
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    International Journal of Chemical Kinetics 16 (1984), S. 543-558 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm Cl}\,\, + \,\,{\rm RI} \to {\rm ICI}\,\, + \,\,{\rm R} $$\end{document} (R = CF3, C2F5, and i,-C3F7) have been studied competitively in the gas phase over the range of 27-231°C. The following Arrhenius parameters were obtained: Textlog A,(cm3/mol · s)E,(kJ/mol)R = CF313.99 ± 0.2117.1 ± 2.0R = C2F513.97 ± 0.2011.5 ± 2.0R = i,-C3F714.18 ± 0.2010.2 ± 2.0The above data lead to bond dissociation energies D(R-I) which are compared with previous published results. The following values are recommended: D,(CF3-I) = 224, D,(C2F5-I) = 219, and D,(i,-C3F7-I) = 215 kJ/mol.
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    International Journal of Chemical Kinetics 16 (1984), S. 603-620 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of methyl radicals (Me) with hexafluoroacetone (HFA), generated from ditertiary butyl peroxide (dtBP), was studied over the temperature range of 402-433 K and the pressure range of 38-111 torr. The reaction resulted in the following displacement process taking place: where TFA refers to trifluoroacetone. The trifluoromethyl radicals that were generated abstract a hydrogen atom from the peroxide: such that k6a is given by: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}\,\,k_{6{\rm a}} \left( {M^{ - 1} \cdot {\rm s}^{ - 1} } \right)\,\, = \,\,8.2\, \pm \,0.7\, - \,8.9\, \pm \,{{1.3} \mathord{\left/ {\vphantom {{1.3} \theta }} \right. \kern-\nulldelimiterspace} \theta } $$\end{document} where θ = 2.303RT kcal/mol. The interaction of methyl and trifluoromethyl radicals results in the following steps: Product analysis shows that k17/k151/2k161/2 = 2.0 ± 0.2 such that k17 = 1010.4±0.5M-1 · s-1. The rate constant k5 is given by: \documentclass{article}\pagestyle{empty}\begin{document}$$ {{{\rm log}\,\,k_5 } \mathord{\left/ {\vphantom {{{\rm log}\,\,k_5 } {\left( {M^{ - 1} \cdot {\rm s}^{ - 1} } \right)}}} \right. \kern-\nulldelimiterspace} {\left( {M^{ - 1} \cdot {\rm s}^{ - 1} } \right)}}\,\, = \,\,8.0\, \pm \,1.3\, - \,5.1\, \pm \,{{0.7} \mathord{\left/ {\vphantom {{0.7} \theta }} \right. \kern-\nulldelimiterspace} \theta } $$\end{document} It is concluded that the preexponential factor for the addition of methyl radicals to ketones is lower than that for the addition of methyl radicals to olefins.
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    International Journal of Chemical Kinetics 16 (1984), S. 679-695 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of 1 and 2% ethane in krypton has been studied in shock waves by the laser-schlieren technique over 1700-4800 K. For 2400-2800 K an effective zero density gradient is seen following the rapid dissociation of the ethane. Through simulation with various mechanisms it is evident that the high rates for the dissociative recombination reactions of methyl radicals\documentclass{article}\pagestyle{empty}\begin{document}$$ 2{\rm CH}_3 \to {\rm C}_2 {\rm H}_4 + {\rm H}_2 $$ $$ 2{\rm CH}_3 \to {\rm C}_2 {\rm H}_5 + {\rm H} $$\end{document}obtained in recent shock-tube studies, are incompatible with this observation; these rates must be reduced at least an order of magnitude. On the basis of theory and previous low-temperature (T) measurements, k = 7.8 × 1011 (-6562/T) (cm3/mol s) is recommended for the second of these reactions.
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    International Journal of Chemical Kinetics 16 (1984), S. 741-752 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of hydrogen atoms produced by the mercury-photosensitized decomposition of H2 with bis(trifluoromethyl)disulfide has been studied. The rate coefficient for the primary reaction, H + CF3SSCF3 → CF3SH + CF3S, was determined in competition with the reaction H + C2H4S → SH + C2H4 to have the value k = (3.0 ± 0.18) × 1014 exp[-(4560 ± 140)/RT] cm3 mol-1 S-1. The high A factor can be partially accounted for by assuming free rotation for the two CF3 groups and the SCF3 groups about the S - S bond in the transition state. The relatively high activation energy is attributed to inductive and orbital overlap effects. CH3SH, H2S, and CF3SH all react with CF3SSCF3 to yield solid complexes which were not explored further.
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    International Journal of Chemical Kinetics 16 (1984), S. 753-766 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of azoethane (AE) was studied by detailed product analysis in the temperature and pressure intervals 508-598 K and 2.7-13.3 kPa. Besides the hydrocarbon products, three characteristic and quantitatively important nitrogen-containing compounds were also determined: ethyl-2-butyldiimide, ethanal-diethylhydrazone, and tetraethyl-hydrazine. Apart from the predominant termination reactions of the ethyl radical with itself and with the μ2 radical, the decomposition is characterized by a very short chain reaction. The measurements led to determination of the following rate constants and rate constant ratios:\documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{rcl} {\rm log}(k_1 /S^{ - 1} ) &=& (16.0 \pm 0.2) - (207.6 \pm 2.0){\rm kJ mol}^{ - 1} /2.3RT\\ log(k_4 /k_3^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} {\rm dm}^{{3 \mathord{\left/ {\vphantom {3 2}} \right. \kern-\nulldelimiterspace} 2}} {\rm mol}^{{{ - 1} \mathord{\left/ {\vphantom {{ - 1} 2}} \right. \kern-\nulldelimiterspace} 2}} s^{{{ - 1} \mathord{\left/ {\vphantom {{ - 1} 2}} \right. \kern-\nulldelimiterspace} 2}} ) &=& (3.3 \pm 0.1) - (54.3 \pm 1.3){\rm kJ mol}^{ - 1} /2.3RT \\ \log (k_5 /k_3^{1/2} {\rm dm}^{{3 \mathord{\left/ {\vphantom {3 2}} \right. \kern-\nulldelimiterspace} 2}} {\rm mol}^{{{ - 1} \mathord{\left/ {\vphantom {{ - 1} 2}} \right. \kern-\nulldelimiterspace} 2}} {\rm s}^{{{ - 1} \mathord{\left/ {\vphantom {{ - 1} 2}} \right. \kern-\nulldelimiterspace} 2}} ) &=& (3.0 \pm 0.1) - (33.7 \pm 1.4){\rm kJ mol}^{ - 1} /2.3RT \\ k_{11} /k_{12} &=& 1.3 \pm 0.1 \end{array} $$\end{document} for the following reactions:
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    International Journal of Chemical Kinetics 16 (1984), S. 793-799 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Boiling-temperature measurements have been used to study the kinetics of the decomposition of urea. Values for the rate constants in neutral, acid, and basic media have been obtained and compared with literature data. The effect of the reverse reaction on the value of the experimental rate constants is discussed. The profile of the ebulliometric curves is different for the three media and is correlated with the number of various species present in solution. It is concluded that ebulliometric measurements can be useful for kinetic studies.
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    International Journal of Chemical Kinetics 16 (1984), S. 817-834 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of hydrogen oxidation near the lower explosion limit in the kinetic region of chain termination has been studied. Major effects, causing deviations of the reaction kinetics from calculations by the linear theory of branched chain processes, are shown to be (1) the inhibition of the reacting mixture by the products of interaction of active centers with vacuum grease or with impurities contained in it and (2) the heterogeneous negative interaction of reaction active centers. The kinetics of hydrogen oxidation in this region has been calculated with consideration of the heterogeneous negative chain interaction. A set of parameters has been obtained that make it possible to determine by the shape of the kinetic curves the sign and the value of nonlinear interaction of chains near the lower explosion limit. It has been shown that the experimental data are in good agreement with the calculations, provided the heterogeneous negative chain interaction is taken into consideration and the inhibiting effect of impurities is eliminated. The rate of heterogeneous generation of chains on a quartz surface treated with hydrofluoric or boric acid has been determined.
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    International Journal of Chemical Kinetics 16 (1984), S. 423-443 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods are described for including the participation of bound electronically excited states in calculations on radical recombination reactions. These methods are illustrated by applying them to the reactions \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm O}\left( {^{\rm 3} P} \right)\,\, + \,{\rm O}\left( {^{\rm 3} P} \right)\,\, + \,\,{\rm M} \to {\rm O}_{{\rm 2}\,} \,\, + \,\,{\rm M}\,} \\ {{\rm O}\left( {^{\rm 3} P} \right)\,\,\, + \,\,{\rm NO}\left( {{\rm X}^{\rm 2} {\rm II}} \right)\, + \,\,{\rm M} \to {\rm NO}_{{\rm 2}\,} \,\, + \,\,{\rm M}} \\ {{\rm OH}\left( {{\rm X}^{\rm 2} {\rm II}} \right)\,\, + \,\,{\rm NO}_{\rm 2} \left( {\tilde X^2 A_1 } \right)\, + \,\,{\rm M} \to {\rm HNO}_{3\,} \,\, + \,\,{\rm M}\,\,\,} \\ \end{array} $$\end{document} For O2, accurate ab initio potentials are used in calculations which show that the electronic degeneracy and long-range part of the potential are likely to be crucial in determining the contribution of a given electronic state to the overall reaction, as long as the state is not so weakly bound that it dissociates thermally before being electronically quenched. Weak collision effects are allowed for using a Monte Carlo technique and an assumed exponential form for the distribution of energies transferred in collisions with a third body. For larger systems it is evident that the role of bound excited states in the low-pressure regime falls rapidly as the size of the system increases. As the high-pressure limit is approached, however, the contribution of excited states is likely to come close to that expected simply on the basis of electronic degeneracy.
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    International Journal of Chemical Kinetics 16 (1984), S. 469-481 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative rate constants for the reaction of OH radicals with a series of branched alkanes have been determined at 297 ± 2 K, using methyl nitrite photolysis in air as a source of OH radicals. Using a rate constant for the reaction of OH radicals with n-butane of 2.58 × 10-12 cm3/molecule · s, the rate constants obtained are (× 1012 cm3/molecule · s): isobutane, 2.29 ± 0.06; 2-methylbutane, 3.97 ± 0.11; 2,2-dimethylbutane, 2.66 ± 0.08; 2-methylpentane, 5.68 ± 0.24; 3-methylpentane, 5.78 ± 0.11; 2,2,3-trimethylbutane, 4.21 ± 0.08; 2,4-dimethylpentane, 5.26 ± 0.11; methylcyclohexane, 10.6 ± 0.3; 2,2,3,3-tetramethylbutane, 1.06 ± 0.08; and 2,2,4-trimethylpentane, 3.66 ± 0.16. Rate constants for 2,2-dimethylbutane, 2,4-dimethylpentane, and methylclohexane have been determined for the first time, while those for the other branched alkanes are in generally good agreement with the literature data. Primary, secondary, and tertiary group rate constants at room temperature have been derived from these and previous data for alkanes and unstrained cycloalkanes, with the secondary and tertiary group rate constants depending in a systematic manner on the identity of the neighboring groups. The use of these group rate constants, together with a previous determination of the effect of ring strain energy on the OH radical rate constants for a series of cycloalkanes, allows the a priori estimation of OH radical rate constants for alkanes and cycloalkanes at room temperature.
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    International Journal of Chemical Kinetics 16 (1984), S. 1227-1246 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of O3 with ethylene, allene, 1,3-butadiene, and trans-1,3-pentadiene have been studied in the presence of excess O2 over the temperature range 232 to 298 K. The initial O3 pressure was varied from 4-18 mtorr, and the olefin pressure was varied from 0.1 to 4.5 torr (ethylene), 2.8 to 39.6 torr (allene), 52.7 to 600 mtorr (1,3-butadiene) or 26.2 to 106 mtorr (trans-1,3-pentadiene). The O3 decay was monitored by ultraviolet absorption. The reactions are first order in both O3 and olefin, and the rate coefficients are independent of the O2 pressure. For the O3-ethylene system, various diluent gases (O2, N2, air) were used and the rate coefficients were found to be independent of the nature of the diluent gas. The various rate coefficients fit the Arrhenius expressions (k in cm3 s-1): \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l}{\rm For C}_{\rm 2} {\rm H}_4 :k\{ 232 - 298{\rm K}\} {\rm } = {\rm }(7.72 \pm 0.89){\rm } \times {\rm 10}^{ - 15} \exp [- 5080{\rm } \pm {\rm }60)/RT] \\ {\rm For C}_{\rm 3} {\rm H}_4 :k\{ 252 - 298{\rm K}\} {\rm } = {\rm }(1.54 \pm 0.25){\rm } \times {\rm 10}^{ - 15} \exp [- 5343{\rm } \pm {\rm }87)/RT] \\ {\rm For 1,3 - C}_{\rm 4} {\rm H}_{\rm 6} :k\{ 254 - 299{\rm K}\} {\rm } = {\rm }(2.20 \pm 0.44){\rm } \times {\rm 10}^{ - 14} \exp [- 4828{\rm } \pm {\rm }109)/RT] \\ {\rm For trans - 1,3 - C}_{\rm 5} {\rm H}_{\rm 8} :k\{ 238 - 298{\rm K}\} {\rm } = {\rm }(1.07 \pm 0.25){\rm } \times {\rm 10}^{ - 13} \exp [- 4608{\rm } \pm {\rm }122)/RT] \\ \end{array}$$\end{document} where the reported uncertainties are one standard deviation and R is in cal/mol K.
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    International Journal of Chemical Kinetics 16 (1984), S. 1257-1266 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The problem of diethanolamine (DEA) degradation in gas-treating processes was quantified through a detailed kinetic study. This reaction was found to be catalyzed by CO2, and degradation occurs in a successive manner to 3-(2-hydroxyethyl)oxazolidone-2, to N,N,N′-tris(2-hydroxyethyl)ethylenediamine and then to N,N′-bis(2-hydroxyethyl)piperazine. A reaction mechanism consistent with these observations was proposed and tested through kinetic analyses. A satisfactory kinetic model which can be of practical use was derived.
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    International Journal of Chemical Kinetics 16 (1984) 
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    Keywords: Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology
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    International Journal of Chemical Kinetics 16 (1984), S. 591-602 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of CCl3 with O(3P) and O2 and those of CCl3O2 with NO have been studied at 295 K using discharge flow methods with helium as the bath gas. The rate coefficient for the reaction of CCl3 with O was found to be (4.2 ± 0.6) × 10-11 cm3/s and that for CCl3O2 with NO was (18.6 ± 2.8) × 10-12 cm3/s with both coefficients independent of [He]. For reaction between CCl3 and O2 the rate coefficient was found to increase from 1.51 7times; 10-14 cm3/s to 7.88 × 10-14 cm3/s as the [He] increased from 3.5 × 1016 cm-3 to 2.7 × 1017 cm-3. There was no evidence for a direct two-body reaction, and it is concluded that the only product of this reaction is CCl3O2. Examination of these results for CCl3 + O2 in terms of current simplified falloff treatment suggests that the high-pressure limit for this reaction is ∼ 2.5 × 10-12 cm3/s, which may be compared with a direct measurement of the high-pressure limit of 5 × 10-12 cm3/s. A value of (5.8 ± 0.6) × 10-31 cm6/s has been obtained for k0, the coefficient in the low-pressure region. This value is compared with corresponding values found earlier for the (CH3, O2) and (CF3, O2) systems and with estimates based on unimolecular rate theory.
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    International Journal of Chemical Kinetics 16 (1984), S. 633-653 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We report laser absorption measurements of NH3 decay within the flame front region of rich, atmospheric pressure ammonia flames. These data are combined with earlier OH, NH, and NH2 measurements to obtain new estimates for the oscillator strength of NH2. This value, fi = 6.4 × 10-5 for the PQ1,7 line in the (0,9,0) ← (0,0.0) vibrational band of the A2A1 ← X2B1 transition, suggests ΔH°f(NH) ≅ 87 kcal/mol. The ammonia profiles were also combined with previous data on NO, NH, NH2, and OH to provide an extensive database at fuel equivalence ratios (ø) of 1.28, 1.50, and 1.81 for comparison to our kinetic model predictions. This modeling used a one-dimensional flame code which explicitly accounts for the diffusional component in our flame experiments. Modeling results using a conventional mechanism predicted concentration profiles which deviated markedly from our observations. It was possible to obtain much more satisfactory fits by postulating reactions between various NHi (i = 1, 2) species to form N - N bonds. The N2Hj (j = 1-3) species could then lose H atoms via dissociation to ultimately form N2. Inclusion of these reactions in the mechanism allowed us to predict concentration - distance profiles for five different species at three different equivalence ratios that are in good agreement with experiment. The most important component of this mechanism is the recognition that the NHi + NHi reactions dominate the kinetics in rich flames. A most satisfying aspect of these calculations is that the key rate constants in the NHi + NHi sequence were estimated using simple RRK theory.
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    International Journal of Chemical Kinetics 16 (1984), S. 1471-1479 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal curves obtained simultaneously at constant heating rates were used to study calcination of ZnCO3 in air. Carroll and Manche's technique, Reich's equation, and Kissinger's method gave an average value for the activation energy of 23 kcal/mol. On the other hand, Coats and Redfern's technique showed the activation energy and preexponential factor to vary over wide ranges. They increase to a maximum and decrease again on increasing the temperature. Their values decrease as the heating rate was increased. One-dimensional diffusion mechanism, obeying parabolic law, may control the entire calcination process.
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    International Journal of Chemical Kinetics 16 (1984), S. 1519-1529 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recombination reaction O + O2 → O3 was studied by laser flash photolysis of pure O2 in the pressure range 3-20 atm, and of N2O—O2 mixtures in the bath gases Ar, N2, (CO2, and SF6) in the pressure range 3-200 atm. Fall-off curves of the reaction have been derived. Low-pressure rate coefficients were found to agree well with literature data. A high-pressure rate coefficient of k∞ = (2.8 ± 1.0) × 10-12 cm3 molecule-1 s-1 was obtained by extrapolation.
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    International Journal of Chemical Kinetics 16 (1984), S. 1557-1566 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficient for the reaction of the hydroxyl radical, OH, with propane has been measured at 1220 K in shock tube experiments, and a value of (1.58 ± 0.24) × 1013 cm3/mol s was obtained. This measured value is compared with previous experimental results and a transition-state theory calculation.
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    International Journal of Chemical Kinetics 16 (1984), S. 1575-1583 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the unimolecular decomposition of phenyl acetate into phenol and ketene, reaction (1): \documentclass{article}\pagestyle{empty}\begin{document}$${\rm PhOCOCH}_3 \buildrel 1\over\rightarrow{\rm PhOH} + {\rm CH}_2 = {\rm C} = {\rm O}$$\end{document} has been studied under very low-pressure conditions between 950 and 1120 K. In this range alternative processes such as the Fries rearrangement to o-hydroxyacetophenone or bond fission into phenoxyl and acetyl radicals are not observed. Based on present and previous evidence a novel four-center transition state is proposed for reaction (1) which corresponds to the high-pressure Arrhenius expression log (k1, s-1) = 12.8 - 56.2/θ, θ = 4.575 × 10-3T kcal/mol.
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    International Journal of Chemical Kinetics 16 (1984), S. 1609-1621 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficient, k, of the reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm H}_2 {\rm O} + {\rm CN} \to {\rm HCN} + {\rm OH} $$\end{document} has been determined in the temperature range 2460-2840 K using a shock tube technique. C2N2—H2O—Ar mixtures were heated behind incident shock waves and the CN and OH concentration time histories were monitored simultaneously using broad-band absorption near 388 nm (CN) and narrow-line laser absorption at 306.67 nm (OH). The rate coefficient expression providing the best fit to the data was \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2.3{\rm} \times {\rm 10}^{{\rm 13}} \exp (- 6700/T){\rm cm}^3 /{\rm mol s} $$\end{document} with uncertainty limits of about ±45% in the temperature range 2460-2840 K. The rate coefficient of the reverse reaction was calculated using detailed balancing, and its extrapolation to lower temperatures was compared with previously published results.
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  • 148
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    Keywords: Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology
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  • 149
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    International Journal of Chemical Kinetics 13 (1981), S. 1-6 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 5-Chloro-2-methylpent-2-ene decomposes at temperatures of 370-420°C with initial pressures from 61to 158 torr to yield hydrogen chloride and a mixture of methylpentadiene isomers. In a static system, with seasoned vessel and propene inhibitor, the reaction is homogeneous, unimolecular, and of the first order. The rate coefficient is expressed by the following Arrhenius equation: log k (sec-1) = (13.43 ± 0.30) - (215.0 ± 3.7) kJ/mol/2.303RT. The result ofthe present work additionally supports the participation of the neighboringaliphatic olefinic double bond in the rate of HCl elimination of alkenyl chlorides in the gas phase. Moreover, it also confirms the three-membered conformation as the most favored structure for anchimeric assistance.
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  • 150
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    International Journal of Chemical Kinetics 13 (1981), S. 59-67 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mixture of Br2 + HBr + C2F5I was photolyzed in the vapor phase. The reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm Br + C}_{\rm 2} {\rm F}_{\rm 5} {\rm I} \to {\rm IBr + C}_{\rm 2} {\rm F}_{\rm 5} $$\end{document} forms C2F5 radicals which are removed by Competitive studies over the range of 74-146°C gave ratios of k10/k9, and these were combined with values obtained previously by different methods at higher temperatures upto 515°C to give \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}k_{10} /k_9) = (- 0.47 \pm 0.03) - (12,500 \pm 300)/\theta $$\end{document} where θ = 2.303RT J/mol. A value is assigned to the activation energy E10, and this, with other data, leads to \documentclass{article}\pagestyle{empty}\begin{document}$$ D{\rm (C}_{\rm 2} {\rm F}_{\rm 5} - {\rm H}) = 429.8 \pm 2.1{\rm KJ}/{\rm mol} $$\end{document} at 25°C. This result is in excellent agreement with two previous independent determinations.
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    International Journal of Chemical Kinetics 13 (1981), S. 97-107 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stoichiometric and, in most cases, absolute rates of coupling of a series of m- and p-substituted benzenediazonium ions with 2,3-dihydroxynaphthalene-6-sulfonate ion (1) have been determined (i) at pH 5.6 (when one OH group is partly monoionized) and (ii) at pH 9.9 (when one OH group is completely ionized and the second slightly so). The rates at both pH values correlate with the σ+ parameter (except for the most reactive ArN2+ at pH 9.9) and the contributions of the two reactive forms of the coupler evaluated. Detailed pH dependences of the coupling rate of the p-chlorobenzenediazonium ion with (1) reveal a strong interaction between (1) and the borate ion, which strongly influences the coupling rate. Coupling rates have also been measured for both diazonium ions and couplers of importance in the diazo reprographic process.
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    International Journal of Chemical Kinetics 13 (1981), S. 187-197 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of several novel elementary reactions involving ClO, BrO and SO free radicals in their ground states were studied in a discharge-flow system at 295 K, using mass spectrometry. The rate constant k2 was determined from the decay of SO radicals in the presence of excess ClO radicals: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm SO} + {\rm ClO} \to {\rm SO}_{\rm 2} + {\rm Cl;}} & {k_{\rm 2} = (2.3{\rm } \pm {\rm 0}{\rm .6}) \times 10^{ - 11} {\rm cm}^3 \sec ^{ - 1} } \\ \end{array}$$ \end{document}The SO + OClO overall reaction has a complex mechanism, with the primary step having a rate constant k5 equal to (1.9 ± 0.7) × 10-12 cm3 sec-1: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm SO} + {\rm OClO } \to {\rm SO}_{\rm 2} + {\rm ClO} $$\end{document}A lower limit for the rate constant of the rapid reaction of SO radicals with BrO radicals was determined: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm SO} + {\rm BrO} \to {\rm SO}_{\rm 2} + {\rm Br;}} & {k_{17} } \\ \end{array} \ge 4 \times 10^{ - 11} {\rm cm}^3 \sec ^{ - 1} $$\end{document}
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  • 153
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    Topics: Chemistry and Pharmacology
    Notes: Gamma radiation-induced free radical chain reactions in liquid mixtures of BrCH2CN, eyelohexane (RH), and haloalkanes (XCCl3) were studied. The kinetics of hydrogen and chlorine atom abstraction from CHCl3, CH3CCl3, CH2ClCCl3, CHCl2CCl3, CF3CCl3, C2Cl6, CCl3CN, and CCl4 by CH2CN radicals were investigated by a competitive method. The reactions investigated were Rate constant ratios k3/k2, k5/k6, k7/k2, and k3/k7 were determined at 180°C. In the CCl4—RH—BrCH2CN system k3/k2 was determined in the temperature range of 100-180°C, yielding log k2 k3 = -0.11 ± 0.2 -(3.34 ± 0.39/θ): where θ = 2.3RT in kcal/mol. The value E2—E3 was combined with existing data on E3 to yield E2(CCl4) = 17.57 kcal/mol. The reactivity trend of CH2CN is compared with that of R radicals. It is shown that in spite of a difference of about four orders of magnitude in kCl values, the reactive cyclohexyl radical is somewhat more selective than CH2CN. It is proposed that the relative reactivities log[k2(XCCl3)/k2(CH3CCl3)] can be correlated in terms of a dual-parameter Taft equation which takes into account both resonance and inductive substituent effects.
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    International Journal of Chemical Kinetics 13 (1981), S. 295-301 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The overall rate constant for hydrogen-atom addition to isobutene has been measured in the temperature range of 298-563 K in a flow discharge system coupled to a quadrupole mass spectrometer. Previously published results allow the determination of \documentclass{article}\pagestyle{empty}\begin{document}$$ \log {\rm }k_1 ({\rm cm}^3 /{\rm mol\,\, sec}) = 13.59 \pm 0.11 - 1.79 \pm 0.19\,\,{\rm kcal/mol/(2}{\rm .3}RT{\rm)} $$\end{document} where the error limits are 95% confidence limits.
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    International Journal of Chemical Kinetics 13 (1981), S. 555-564 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of acid catalyzed decomposition of peroxodisulfate, (S2O82-) in aqueous perchlorate medium involves the hydrolysis of the species H2S2O8 and HS2O8- and the homolysis of the species H2S2O8, HS2O8- and S2O82- at the O—O bond. The overall rate law when 1.4M 〉 [HClO4] 〉 0.1M is \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{ - d[{\rm S}_{\rm 2}{\rm O}_8^{2 - }]}}{{dt}}\, = \,k_0 [{\rm S}_{\rm 2}{\rm O}_8^{2 - }]\, + \,k' [{\rm S}_{\rm 2}{\rm O}_8^{2 - }][{\rm H}+]\, + \,k{''}[{\rm S}_{\rm 2}{\rm O}_8^{2 - }][{\rm H}+]^2 $$\end{document}The constants k′ and k″ contain the hydrolysis and homolysis rate constants of HS2O8- and H2S2O8, respectively. With added Ag(I), the acid catalyzed and Ag(I) catalyzed reactions take place independently. Ag(I) catalyzed decomposition appears to involve the species AgS2O8- (aq).
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    International Journal of Chemical Kinetics 13 (1981), S. 543-554 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolysis of C2H5I in a glassy salt matrix (5M, 7.5M, 10M) of aqueous LiCl at 77 K with light of λ = 254 nm has been conducted, product analysis being by ESR and UV spectroscopy. The electrolytic medium causes the ionization of product HI, and I- concentrations can be continuously determined. During photolysis [I-] is less than the amount of C2H5I decomposed. But after photolysis thaw-freeze cycling is accompanied by progressive growth in [I-] until the yield matches the C2H5I loss, the quantum yields being 0.26, 0.20, and 0.17 for the three LiCl solutions, respectively. The quantum yield of unionized HI is unchanged, however, at around 0.36, the overall change being due to a fall in the extent to which the HI is ionized in the direct photolysis (ø = 0.22, 0.16, and 0.11). It is proposed that this is a consequence of the density increase of matrix packing as the LiCl concentration is increased so that fewer HI are in contact with the aqueous medium and cage recombination is favored.The results establish that the primary reaction is essentially exclusive: and that substantial aggregates of C2H5I exist within which HI are caged and cannot be ionized. The direct reaction \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm C}_{\rm 2}{\rm H}_{\rm 5}{\rm I}+ h\nu \to {\rm C}_{\rm 2}{\rm H}_5^. + {\rm I}^. $$\end{document} occurs only to a trivial extent, ø; = 10-4, C2H5 arising virtually totally via \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm C}_{\rm 2}{\rm H}_{\rm 4}+ {\rm H}^. \to {\rm C}_{\rm 2}{\rm H}_5^. $$\end{document}
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    International Journal of Chemical Kinetics 13 (1981), S. 577-589 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis kinetics of 4,4-dimethylpent-2-yl acetate, in a static system and in a vessel seasoned with allyl bromide, have been studied in the temperature range of 300-350°C and the pressure range of 48-211 torr. The olefin products were 4,4-dimethylpent-1-ene, cis-4,4-dimethylpent-2-ene, and trans-4,4-dimethylpent-2-ene. The rate coefficient for the homogeneous unimolecular elimination of this ester is given by the following Arrhenius equation: log k(sec-1) = (12.87 ± 0.31) - (181.2 ± 3.4)kJ/mol/2.303RT. The direction of elimination of this acetate has been found to proceed to the formation of the corresponding olefin by kinetic control. The present data, together with other pyrolysis work subject to kinetic control, imply that the direction of elimination of bulky alkyl esters is determined by steric hindrance in the eclipsed cis conformation. However, further analyses reveal that if a series of esters are compared, in the case of a gradual increase of alkyl branching when adjacent to a hydrogen atom (alkyl-H interactions), the rate was determined by steric acceleration, owing to the crowding effect at the highly substituted carbon atom. Otherwise if this gradual alkyl increase in size happened to be adjacent to another alkyl substituent (alkyl-alkyl interactions), the rate was affected by steric hindrance of the eclipsed cis conformation.
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    International Journal of Chemical Kinetics 13 (1981), S. 651-665 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For H-atom abstraction reactions by HO radicals it has been shown that If Di is taken as the C—H bond dissociation enthalpy at 298 K, then a = 0.323 and D0is obtained from the empirical formula \documentclass{article}\pagestyle{empty}\begin{document}$$ D_0 ^{ - 1} = 1.062 \times 10^{ - 2} + 3.52 \times 10^{ - 6} T $$\end{document} where D0 is in kcal/mol and T is in K. Thisrelationship is valid for T between 200 and 400 K. Finally empiricalrelationships are given to help estimate Di.
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    International Journal of Chemical Kinetics 13 (1981), S. 677-691 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bimolecular rate constant for the title reaction has been measured by very-low-pressure reactor techniques at 233 〈 T K 〈 338. The equilibrium constant has also been measured between 253 and 338 K. Our rate constants are in excellent agreement with recent measurements using very different techniques and reaction conditions, and the general agreement probably makes this one of the most accurately measured rateconstants. Transition state models of the reaction rule out a bent TS in favor of a TS with colinear Cl···H···C bonds. The curvature at higher temperatures (〉350 K) is quantitatively accounted for by transition state theory analysis. Tunneling is shown not to play a role. The measured values of K1 allow an experimental value of S° (CH3) to be fixed to only ±2.4 e.u. However, using known values of S° for all species gives ΔH°f298(CH3.) = 35.1 plusmn; 0.1 kcal/mol in excellent agreement with other measured values.
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    International Journal of Chemical Kinetics 13 (1981), S. 735-740 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of NOx-air irradiations, with trace amounts of propane and propene present to monitor OH radical concentrations, have been carried out in a 5800-L evacuable environmental chamber to investigate radical levels and sources during such irradiations. The data obtained show conclusively that unknown radical sources are present, and that photolysis of initial nitrous acid can be, at best, only a minor source of radicals after ∼30-60 min of irradiation.
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    International Journal of Chemical Kinetics 13 (1981), S. 755-770 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of cyclopentyl cyanide has been investigated in the temperature range of 905-1143 K using both conventional stirred-flow reactor and very low-pressure pyrolysis (VLPP) techniques. The results from both techniques are consistent. The main primary processes are HCN elimination to form cyclopentene: and ring fragmentation to form vinyl cyanide plus propylene and ethylene plus cyanopropenes: Under the experimental conditions cyclopentene undergoes further decomposition to cyclopentadiene plus hydrogen. There is evidence for conversion of some of the reactant to a solid residue, presumably polymer. From the stirred-flow reactor results the following Arrhenius expressions were obtained: log k1(s-1) = (12.8 ± 0.3) - (65.6 ± 1.3)/θ and log k2(s-1) = (16.0 ± 0.3) - (80.0 ± 1.1)/θ, where θ = 2.303RT kcal/mol. Application of RRKM theory shows that the VLPP experimental rate constants are consistent with high-pressure Arrhenius parameters given by log k1(s-1) = (12.8 ± 0.3) - (67.8 ± 2.5)/θ for HCN elimination, and log k4(s-1) = (16.3 ± 0.3) - (80.1 ± 2.0)/θ for the sum of the ring fragmentation pathways. The rate parameters for HCN elimination are in good agreement with previous VLPP studies of alkyl cyanides and with theoretical predictions. The difference in activation energies for the ring opening of cyclopentane and cyclopentyl cyanide is reasonably close to the established value for the cyano stabilization energy. This supports the assumption of a biradical mechanism.
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    International Journal of Chemical Kinetics 13 (1981) 
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    International Journal of Chemical Kinetics 13 (1981), S. 23-38 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and mechanism of the free-radical chain dechlorination of C2Cl6, C2Cl5H, and sym-C2Cl4H2 in Et3SiH wereinvestigated over a wide temperature range. The propagation step of the dechlorination of chloroethanes (C2Clx H6-x) proceeds by the following reactions: Analysis of the temperature dependence of product formation gave the Arrhenius expressions for k4/k3 which in turn were utilized for the estimation of the absolute Arrhenius parameters for hydrogen abstraction from Et3SiH. Our results show that the values of Eabs are lower in Et3SiH than in c-C6H12 by about 2-3 kcal/mol, while the A factors are almost equal. In competitive studies k2 was determined versus Br abstraction from n-C5H11Br. The relative Arrhenius parameters determined by this method show that variations in both A factors and activationenergies are responsible for the reactivity trends observed in the Cl transfer reactions of Et3Si radicals.
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    International Journal of Chemical Kinetics 13 (1981), S. 85-96 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of dimethyl, dipropyl, and diphenyl sulfides by pyridinium chloro chromate in chlorobenzene-nitrobenzene mixtures are reported. The rate data show Michaelis-Menten behavior. The oxidation process is catalyzed by the organic acids like dichloro and trichloro acetic acids. The rate-determining step appears to be a unimolecular decomposition of a complex of the reactants.
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    International Journal of Chemical Kinetics 13 (1981), S. 111-118 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants of peroxy radical recombination in the oxidation of 1-methyl-3-phenylindan, 1,3-dimethyl-3-phenylindan, and 1,1-dimethyl-3-phenylindan were measured using the nonstationary-state technique. A cooxidation method was applied to obtain the reactivities of these compounds with respect to α-phenylethyl peroxy radicals.
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    International Journal of Chemical Kinetics 13 (1981), S. 173-186 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two-parameter equation correlations are reported for radical reactions of aromatic compounds. In these correlations polar and resonance substituent constants identical with the substituent constants of aliphatic compounds were used. The equations correlate the rate constants for H abstraction reactions and for the addition of a variety of free radicals to the ortho-, meta-, and para-substituted aromatic compounds. Besides, they correlate parameters of the spectra for substituted aromatic radicals. The correlations show that the effects of para substituents on the reactions studied are nearly entirely resonance effects, whereas for the meta- and ortho-substituted compounds polar (inductive) effects become essential. Application of the two-parameter correlations permits also to determine the structure of transition states (σ or π-complex) in free-radical reactions.
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    International Journal of Chemical Kinetics 13 (1981), S. 199-207 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results on the oxidation of N3- by Br2 in neutral and acid media are presented. The rate of the reaction is found to be proportional to [N3-] and [Br2]. The gaseous product of oxidation is found to be pure nitrogen. The stoichiometry of the reaction is \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm Br}_2 + 2{\rm N}_{\rm 3}^ - \to 2{\rm Br}^ - + 3{\rm N}_{\rm 2} {\rm ([N}_{\rm 3}^ -]) 〉 [{\rm Br}_2] $$\end{document} The reaction shows a positive salt effect. It is found that the addition of Br- stabilizes the complex BrN3, which decomposes into Br- and N2: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm Br}_2 + {\rm N}_{\rm 3}^ - \rightleftharpoons {\rm BrN}_{\rm 3} + {\rm Br}^ - } \\ {{\rm BrN}_3 + {\rm N}_{\rm 3}^ - \to {\rm Br}^ - + 3{\rm N}_{\rm 2} } \\ \end{array} $$\end{document} The spectroscopic measurements also support the kinetic observation. The equilibrium constant K, the rate constants and the thermodynamic parameters were calculated. It is observed that H+ ion inhibits the reaction. The mechanism is discussed in terms of the kinetic results.
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    International Journal of Chemical Kinetics 13 (1981), S. 245-254 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal unimolecular decomposition of pent-1-yne has been investigated over the temperature range of 923-1154 K using the technique of very low-pressure pyrolysis (VLPP). Under the experimental conditions the reaction proceeds predominantly via a molecular retro-ene pathway to yield allene and ethylene. There was some evidence for the occurrence of the higher energy C3—C4 bond fission pathway at the high end of the temperature range. Interpretation of the data with the aid of RRKM theory and taking into account a decrease in gas-wall collision efficiency with temperature yields the following high-pressure rate constant expression for the retro-ene pathway: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k(\sec ^{ - 1}) = (12.8 \pm 0.4) - (57.0 \pm 2.0)/\theta $$\end{document} at 1100 K where θ = 2.303 RT kcal/mol and the A factor was assigned from the results of shock-tube studies of similar molecules. These rate parameters are independent of the inclusion of the bond fission pathway in the RRKM calculations. The results are compared with previous data on the retro-ene decomposition of alkynes.
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    International Journal of Chemical Kinetics 13 (1981), S. 273-282 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal unimolecular decomposition of hex-1-yne has been investigated over the temperature range of 903-1153 K using the technique of very low-pressure pyrolysis (VLPP). The reaction proceeds via the competitive pathways of C3—C4 fission and molecular retro-ene decomposition, with the latter being the major pathway under the experimental conditions. RRKM calculations, generalized to take into account two competing pathways, show that the experimental unimolecular rate constants are consistent with the high-pressure Arrhenius parameters at 1100 K given by \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k(\sec ^{ - 1}) = (12.7 \pm 0.4) - (56.4 \pm 1.0)/\theta \;\;\;\hbox{for retro-ene} $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k(\sec ^{ - 1}) = (15.9 \pm 0.3) - (70.7 \pm 2.0)/\theta \;\;{\rm for}\;{\rm C} {-} {\rm C}\,{\rm fission} $$\end{document} where θ = 2.303 RT kcal/mol and the A factors were assigned from the results of recent shock-tube studies of hex-1-yne and related alkynes. The results for C—C fission are consistent with previous VLPP and shock-tube determinations of the propargyl resonance energy, and the parameters for the molecular pathway are consistent with systematic trends for the retro-ene decomposition of unsaturated hydrocarbons.
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    International Journal of Chemical Kinetics 13 (1981) 
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  • 171
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    International Journal of Chemical Kinetics 13 (1981), S. 367-384 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis of azo-n-propane and of azoisopropane has been studied by kinetic spectroscopy. Transient absorption spectra in theregion of 220-260 nm have been assigned to the n-propyl and isopropyl radicals. For the n-propyl radical, ∊max = 744 ± 39 l/mol cm at 245 nm and the rate constants for the mutual reactions were measured to be kc = (1.0 ± 0.1) × 1010 l/mol sec (combination) and kd = (1.9 ± 0.2) × 109 l/mol sec (disproportionation). For the isopropyl radical, ∊max = 1280 ± 110 l/mol cm at 238 nm, with kc = (7.7 ± 1.6) × 109 l/mol sec and kd = (5.0 ± 1.2) × 109 l/mol secThe rate constant for the dissociation of the vibrationally excited triplet state of the azopropanes into radicals was measured from the variation in the quantum yield of radicals with pressure. For azo-n-propane kdT = (6.6 ± 1.3) × 107 sec-1, and for azoisopropane kdT = (1.6 ± 0.4) × 108 sec-1. Collisional deactivation of the vibrationally excited singlet and triplet states was found to occur on every collision for n-pentane; but nitrogen and argon were inefficient with a rate constant of 1.1 × 1010 l/mol sec.Spectra observed in the region of 220-260 and 370-400 nm areattributed to the cis isomers of the parent trans-azopropanes. These are formed, as permanent products, in increasing amounts as the pressure is increased.
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    International Journal of Chemical Kinetics 13 (1981), S. 427-432 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions have been studied competitively over the range of 28-182°C by photolysis of mixtures of Cl2 + C2F5I+ CH4. We obtain \documentclass{article}\pagestyle{empty}\begin{document}$$ \log {\rm }k_1 /k_2 = (0.96 \pm 0.06) + (1210 + 440)/\theta $$\end{document} where θ = 2.303RT J/mol. The use of published data on reaction (2) leads to log (k1cm3/mol sec) = (13.96 ± 0.2) - (11,500 ± 2000)/θ.
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  • 173
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    Topics: Chemistry and Pharmacology
    Notes: Rate constants and activation parameters for the isotopic exchange reactions between (PhO)2PSCl and M36Cl (M = Me4N+, Et4N+, n-Bu4N+, Et3HN+, EtH3N+, Li+) in acetonitrile were measured in order to find the effect of the cation nature onthe kinetics of the reaction. The rate constants measured for a range of concentrations of Et3HN36Cl, EtH3N36Cl, and Li36Cl were analyzed using the Acree equation. The equivalent conductance of LiCl in acetonitrile was determined. The nature of the cation has no effect on the mechanism of the reaction. The cation changes only the experimental rate constant proportionally to the dissociation degree of the salt. Smaller values of the rate constant and smaller activation parameters ΔH
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  • 174
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    International Journal of Chemical Kinetics 13 (1981), S. 473-480 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Cl-transfer reaction between CFCl3 and c-C6H11 radicals (R) was studied in liquid cyclohexane (RH). The Arrhenius parameters for Cl abstraction were determined in the RH-CFCl3 system versus the termination reaction between cyclohexyl radicals and competitively versus addition to C2Cl4 in the RH-CFCl3-C2Cl4 system. The two sets of results are in very good agreement and give the following Arrhenius expression for the reaction R + CFCL3 → RCl + CFCl2 (2): \documentclass{article}\pagestyle{empty}\begin{document}$$ \log {\rm }k_2 (1/{\rm mol\, sec}) = 8.95 - 7.79/\theta $$\end{document} where θ = 2.303RT in kcal/mol. Comparison with Cl-transfer data of other chloromethanes and chloroethanes shows that an increase in the C—Cl bond dissociation energy is the main cause of the reduced reactivity of CFCl3. Based on a previously developed correlation, D(CFCl2 — Cl) is estimated to be equal to 74.4 kcal/mol.
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    International Journal of Chemical Kinetics 13 (1981), S. 515-515 
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    Keywords: Chemistry ; Physical Chemistry
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  • 176
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    International Journal of Chemical Kinetics 13 (1981), S. 517-526 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of gamma-radiation induced free radicals reactions in carbon tetrachloride solutions of cyclohexane, cyclooctane and cyclododecane were studied in the range of 27-190°C. The activation energies found were in the order c—C6H12 〉 c—C12H24 〉 c—C8H16, which was explained as due to their ring strain which has the same order. The following log k1 was obtained using the known Arrhenius parameters for CCl3 radical recombination:
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    International Journal of Chemical Kinetics 13 (1981), S. 565-575 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Detailed measurements on the kinetics and stoichiometry of the oxidation of N-methylformamide and N,N-dimethylformamide by aquosilver (II) ions are reported. Four AgaqII ions are consumed for each amide, and the reaction is first order in [AgaqII] and first order in [amide]. The reaction is inversely dependent on acidity in the range of 1.5-5.0M HClO4. The oxidation rate is independent of [AgI] and ionic strength. The proposed reaction mechanism and activation parameters are compared with those found for the oxidation of amides by other oxidants such as cobalt(III) and manganese(III).
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    International Journal of Chemical Kinetics 13 (1981), S. 603-613 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A special method of electrodialysis has been developed for investigation of the kinetics and mechanism of polymerization reactions involving ions. The ionic composition of homogeneous systems such as Cp2TiRClAlRCl2, RTiCl3 + AlRCl2, Ti(OR)4 + AlR3, and (RLi)n has been studied. The composition of catalytically active ions has been determined. Using the regularities of “open” systems, the methods of determining the carbocation reactivity under electrodialysis conditions havebeen worked out. The impulse electrodialysis method has been suggested for studying ionic polymerization kinetics and evaluating the rate constants ofion reactions with the monomer and gegenion.
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    International Journal of Chemical Kinetics 13 (1981), S. 639-649 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the thermal decomposition of CF3O3CF3 has been investigated in the pressure range of 15-599 torr at temperatures between 59.8 and 90.3°C and also in the presence of CO between 42 and 7°C. The reaction is homogeneous. In the absence of CO the only reaction products are CF3O2CF3 and O2. The rate of reaction is strictly proportional to the trioxide pressure, and is not affected by the total pressure, the presence of inert gases, and oxygen. \documentclass{article}\pagestyle{empty}\begin{document}$$ -\frac{{d[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_{\rm 3}]}}{{dt}} = 2\frac{{dp}}{{dt}} = k[{\rm CF}_{\rm 3} {\rm O}_{\rm 3}{\rm CF}_{\rm 3}] $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2.25 \pm 0.18 \times 10^{15} \exp (- 30,530 \pm 130\,{\rm cal}/RT)s^{ - 1} $$\end{document}The following mechanism explains the experimental results: In the presence of CO there appear CO2, (CF3OCO)2, and CF3O2C(O)OCF3 as products. With increasing temperature the amount of peroxicarbonate decreases, while the amounts of oxalate and CO2 increase. The rate of decomposition of the trioxide above a limiting pressure of about 10 torr CO is strictly first order and independent of CO pressure, total pressure, and the pressure of the products. \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_3]}}{{dt}} = k*[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_{\rm 3}] $$\end{document} The addition of larger amounts of O2 to the CO containing system chaqnges the course of the reaction.
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    International Journal of Chemical Kinetics 13 (1981), S. 729-733 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of the title compound has been studied in the gas phase in the temperature range of 584-634 K. The decomposition was found to be a first-order homogeneous process yielding 2-methylbuta-1,3-diene and formaldehyde. The rate constants obtained at 11 temperatures within the quoted range fitted the Arrhenius equation \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}k/({\rm s}^{ - 1}) = 14.619 \pm 0.030 - (209.48 \pm 0.35)\,{\rm kJ}\,{\rm mol}^{ - 1} /RT\,\ln \,10 $$\end{document} The decomposition is probably unimolecular and concerted.
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    International Journal of Chemical Kinetics 13 (1981), S. 771-783 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of hydrogen abstraction from cyclohexene by CCl3 radicals were studied in CCl4 solution as a function of cyclohexene concentration and temperature in the range of 26-140°C. The CCl3 radicals were produced both by radiolysis of CCl4 and by photolysis of CCl3Br. The rate constant for the reaction was found to be given by the equation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k1(M^{ - 1} s^{ - 1}) = 7.64 - 6.36/\theta $$\end{document} where θ = 2.303 RT kcal/mol. This activation energy leads to C—H bond strength for the allylic hydrogen of 85 ± 1 kcal/mol, which means a resonance stabilization energy of 11 ± 1.5 kcal/mol for the C-C6H11 radical.
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    International Journal of Chemical Kinetics 13 (1981), S. 789-798 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An approximate analytical solution of relaxation in a low-pressure system with exponential transition probabilities is given for vibrational-rotational energy transfer in the dissociation of diatomics. The main assumption is that the rotational degrees of freedom are in thermal equilibrium at all times, and that the barrier to dissociation in the vibrational-rotational plane is linear and asymmetric. The theory is applied to high-temperature dissociations of N2, Br2, and CO in excess argon, with satisfactory agreement with available experimental data.
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    International Journal of Chemical Kinetics 13 (1981), S. 845-854 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A preliminary report is given of relative reactive cross sections for four abstraction reactions H + H′Br ← HH′ + Br with attacking atom (A) H or D, and atom under attack (B) H or D. The pattern of reactive cross sections, as obtained in a crossed molecular beam experiment at a collision energy ET = 7 kcal/mol, indicates Sr(D,H) ≤ Sr(D,D) 〉 Sr(H,H) 〉 Sr(H,D). The atoms in parentheses are A and B. We describe a three-dimensional classical trajectory (CT) study on a potential-energy surface proposed in 1969 by Parr and Kuppermann (PK); the CT results are in fair accord with experiment. It is suggested that (D,H) has the largest cross section because it exhibits the most favorable relative timing of A approach to BC rotation. On the basis of CT it appears that the same sequence of cross sections and the same rationale may be applied to the exchange reactions H + BrH′ ← HBr + H′.
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    International Journal of Chemical Kinetics 13 (1981), S. 883-895 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of formation of primary products from cumene cracking over a partially exchanged LaNaY catalyst have been studied at 400, 450, and 500°C. It has been found that in both the fully and the partially exchanged LaNaY zeolite catalysts the nature of active sites is the same. The higher activity of the fully exchanged catalyst is attributed to a higher concentration of the active sites. It has also been found that an increase in exchange level leads to an increase in the number of both Bronsted and Lewis active sites, but in somewhat different proportions. A comparatively slight increase in the decay rate constant is observed over the same increase in the level of exchange.
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    International Journal of Chemical Kinetics 13 (1981), S. 897-911 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initial rates of formation of the major products in the thermal reactions of ethylene at temperatures in the neighborhood of 750 K have been measured in the presence and absence of the additive butene-1. It has been shown that this ratio of rates is related to the ratio of rate constants for the two initiation processes: The ratio k′1/k1 has been measured over the temperature range of 700-773 K and may be expressed as (R = 1.987 cal/mol deg) log k′1k1(mol/L) = 2.8 - 4400/2.3RT. Assuming a value for k′1 of log k′1 (s-1) = 16 - 71,500/2.3RT, the value of k1 may be expressed as log k1(L/mol) = 13.2 - 67,000/2.3RT. The values for the frequency factor and activation energy for reaction (1) are discussed in relation to the heat of formation of the vinyl radical, and it is concluded that reaction (1) is the main initiation process in the thermal decomposition of ethylene under the present conditions.
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    International Journal of Chemical Kinetics 13 (1981), S. 913-923 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cell membranes consist of lipid bilayers in which proteins are embedded. Many cell functions are carried out at the cell boundary which interface with water. Here we describe the response to an anesthetic of a lipid bilayer and of an enzyme separately. While both systems are markedly affected by anesthetics at appropriately high concentrations, the result at the clinical concentrations seems best explained as principally an effect on the protein somewhat accentuated by its presence in the lipid bilayer. Thus the lipoprotein complex seems to have the properties of the protein alone, except with somewhat greater induced sensitivity due to the lipid matrix in which it is immersed.
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    International Journal of Chemical Kinetics 13 (1981), S. 945-956 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A phase-shift method has been used to determine the rate constant for the reaction of ground state oxygen atoms with HCl over the temperature range of 330-600 K. Oxygen atoms were generated by modulated mercury photosensitized decomposition of N2O, and monitored by the chemiluminescence from their reaction with NO. After correction for diffusion of oxygen atoms from the viewing zone, the rate constants can be represented by the Arrhenius equation k1 = (3.06 ± 1.43) × 1012 exp[(-3160 ± 184)/T] cm3/mol·s. The indicated uncertainties are 95% confidence limits for 15 degrees of freedom. Also, the third-body efficiency of HCl relative to N2O in the reaction O + NO + M ← NO2 + M was determined to be 1.9 ± 0.2 over the temperature range of 298-360 K.
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    International Journal of Chemical Kinetics 13 (1981), S. 925-944 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experiments are described in which the kinetics of cathodic hydrogen evolution from the unhydrated H3O+ ion in pure CF3SO3- H3O+ are compared with those from an aqueous solution of CF3SO3H where the proton is mainly in a fully hydrated state as H9O4+. From the acid hydrate, which exists mainly as the ionic compound CF3SO3-H3O+, rates of H2 evolution at Ni, Pt, and Hg electrodes, measured at a given overpotential or expressed as exchange current densities, are between about 3.5 and 20 times slower than those from the same electrolyte in dilute (1.0M) aqueous solution. Allowing for the concentration differences in these two types of system and double-layer effects, the rate constants are between about 9.4 and 216 times smaller for the reaction from H3O+ than from H9O4+ at the above electrodes.The evaluation of apparent heats of activation for H2 evolution from the two types of proton sources allows ratios of real frequency factors to be calculated for discharge from H3O+ and H9O4+. These data have a bearing on the theoretical conclusions regarding proton discharge mechanisms and show that frequency factor effects can be as important as activation energy differences in determining the rates of proton discharge from different proton sources.The results are discussed in terms of current ideas about electron and proton transfer in electrochemical reactions, the state of hydration of H+, and the role of discharge from paired CF3SO3- and H3O+ ions. In particular, the molecular mechanics of discharge of the proton from the molecular ion H3O+ can be different from that from the fully hydrated H+ ion where many more HO- vibrational and librational modes can be involved in the process of activation of the H9O4+ entity.
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    International Journal of Chemical Kinetics 13 (1981), S. 957-975 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quasi-classical trajectory calculations have been performed on the H + O2 system. Significant reaction probabilities are obtained when the initial energy is in rotation or vibration, or a combination of the two, but not when the initial energy is in translation. The opacity function shows a bimodal dependence on the impact parameter, with a small peak at 0.9 Å 〈 b 〈 1.5 Å and a very prominent peak at 2.5 Å 〈 b 〈 3.3 Å. The product scattering angles and product energy distributions also depend on b and to a limited extent on the initial energy distribution.The observations can be largely interpreted in terms of the nature of the motion on the potential energy surface, while the effects of rotational energy on the reaction follow qualitatively from statistical phase-space theory.
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    International Journal of Chemical Kinetics 13 (1981), S. 977-999 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nascent vibrational energy distributions of the HF† formed in the reactions of a series of partially fluorinated alkanes (RFH; RF = CH2F, CHF2, CF3, C2F5, C3F7, and C7F15) with electronically excited oxygen atoms O(21D2) have been determined by measuring the appearance times of stimulated emissions from various vibration-rotation transitions in a grating-tuned optical cavity. The vibrational energy contents of the HF formed in these reactions were found to be considerably greater than statistically expected. These reactions are believed to occur via vibrationally excited short-lived α;-fluorinated alcohols (RFOH†), formed by insertion of the O(21D2) atoms into C—H bonds. The observation of nonstatistical energy partitioning in the above reactions is in clear contrast to the result obtained from the O(21D2) + CF3CH3 reaction that produces the β-fluorinated alcohol CF3CH2OH, from which the HF product carries a near statistical vibrational energy distribution. A mechanism for HF† formation in these very exothermic reactions is presented.
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    International Journal of Chemical Kinetics 13 (1981), S. 1001-1010 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of thiosulfate to tetrathionate by trans-dihydroxotetraoxoosmate(VIII) in aqueous alkaline media have been studied. The oxidation follows a rate expression \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm Os(VIII})]}}{{dt}} = k3{\rm K}_{OS} {\rm K}_2 [{\rm S}_2 {\rm O}_3^{2 - }][{\rm Os(VIII})](1 + {\rm K}_{os} {\rm K}_2 [{\rm S}_2 {\rm O}_3^{2 - }])^{ - 1} $$\end{document} where KOs is the formation constant of trans-dihydroxotetraoxoosmate (VIII), and K2 and k3, respectively, represent the formation constants of the intermediate complex involving Os(VIII) and S2O32- and its decomposition constant. The KOs, K2, and k3 values have been computed to be (19.5 ± 3) dm3/mol, (6.12 ± 0.5) and (3.32 ± 0.3) × 10-1 dm3/mol s at 303 K, and I = 0.32 mol/dm3, respectively. The rate law is consistent with a mechanism envisaging the equilibrium formation of an intermediate complex involving Os(VIII) and S2O32-, followed by a rate-determining decomposition of the complex with concomitant electron transfer.
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    International Journal of Chemical Kinetics 13 (1981), S. 1011-1028 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction between C2H5 and O2 at 295 K has been studied with a flow reactor sampled by a mass spectrometer. With helium as the carrier gas the rate coefficient was found to increase from (1.2 ± 0.3) × 10-12 to (3.6 ± 0.9) × 10-12 cm3/s as [He] was increased from 2 × 1016 to 3.4 × 1017 cm-3. The importance of has been determined from a knowledge of the initial C2H5 concentration together with a measurement of the C2H4 produced in reaction (5). F, the fraction of the C2H5 radicals removed by path (5), was found to decrease from 0.15 to 0.06 as [He] increased from 2 × 1016 to 3.4 × 1017 cm-3. The rate coefficient for reaction (5) was found to be independent of [He] and to have a value of (2.1 ± 0.5) × 10-13 cm3/s. The variation in F reflects the fact that k1b increases as [He] increases. These observations are taken as evidence for a direct mechanism for C2H4 production and a collision-stabilized route for C2H5O2 formation. Calculations indicate that the high-pressure limit for reaction (1b) is ∼4.4 × 10-12 cm3/s and that in the polluted troposphere the branching ratio for reactions (1b) and (5) will be ∼l20.
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  • 195
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1029-1040 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the cerium(IV) oxidation of p-nitro and p-methoxymandelic acids have been investigated in H2SO4-MHSO4 (M+ = Li+, Na+, K+) and H2SO4-MClO4 (M+ = H+, Na+) mixtures at a constant total electrolyte concentration of 2.00 mol/dm3. The oxidation of p+nitromandelic acid proceeds through two [H+]-independent paths, as was also observed for some substituted mandelic acids studied previously. The kinetic behavior of the p-methoxy derivative differs from that of the other mandelic acids in that (1) the oxidation occurs via two [H+]-dependent paths, (2) the reaction rate is anomalously high, (3) the activation enthalpy and entropy of the overall process are markedly lower. It provides strong support to the suggestion that a different mechanism is operative. The substituent effects and the reaction mechanism are discussed.
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  • 196
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    International Journal of Chemical Kinetics 13 (1981), S. 1041-1050 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flash photolysis of CH3CHO and H2CO in the presence of NO has been investigated by the intracavity laser spectroscopy technique. The decay of HNO formed by the reaction HCO + NO → HNO + CO was studied at NO pressures of 6.8-380 torr. At low NO pressure HNO was found to decay by the reaction HNO + HNO → N2O + H2O. The rate constant of this reaction was determined to be k1 = (1.5 ± 0.8) × 10-15 cm3/s. At high NO pressure the reaction HNO + NO → products was more important, and its rate constant was measured to be k2 = (5 ± 1.5) × 10-19 cm3/s. NO2 was detected as one of the products of this reaction. Alternative mechanisms for this reaction are discussed.
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  • 197
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    International Journal of Chemical Kinetics 13 (1981), S. 1051-1070 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A theory of collisional energy transfer based on microcanonical relaxation in the limit of infinitesimal collision lifetimes is developed. In distinction to the recently formulated ergodic collision theory the potential energy is now frozen due to the short time scale, and only kinetic energy is available for redistribution. As a consequence, the rate of energy transfer is decreased, and agreement with experimentally based estimates generally improved.
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  • 198
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    International Journal of Chemical Kinetics 13 (1981), S. 1071-1083 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of hot hydrogen atoms originating from 253.7- and 228.8-nm photolyses of hydrogen sulfide with 1-butene was investigated. Of the hydrogen atoms undergoing addition a substantial part undergoes it in a first collision (37 and 48% at 253.7 and 228.8 nm, respectively) yielding highly excited butyl radicals. The ratio of nonterminal to terminal addition is 0.5 and practically does not depend on the energy of the hydrogen atoms over the range of 15-33 kcal/mol. Comparing the results of 229- and 254-nm photolyses of hydrogen sulfide with those of 313- and 334-nm photolyses of hydrogen iodide with the use of the decomposition rate constants of n-butyl radicals calculated by the RRKM methods, the conclusion is reached that the hydrogen atom from H2S photodissociation has 90-95% of the available energy.
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  • 199
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1101-1103 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 200
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1085-1099 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bimolecular reaction of HI in CO2, which was excited vibrationally by irradiation of a continuous-wave CO2 laser light, was investigated in the temperature range of 721-980 K. An enhancement of the reaction rate by a factor of about 2.5 was observed in the 1:1 HI—CO2 mixture in comparison with the rate in pure HI when both sample gases were irradiated by a CO2 laser (50 W) at 1 torr. However, in the HI-SF6 mixtures the decomposition rate of HI was not accelerated by irradiation of the CO2 laser. Thus the enhancement is attributed to vibrational excitation of HI through collisional energy transfers from laser-excited CO2 (00°1). At lower total pressures or at lower partial pressures of HI in HI-CO2 mixtures the enhancement was more significant because of inefficient vibrational deactivation of excited HI. A model calculation gave the result in agreement with the experimental one if the effective activation energy is assumed as Ea† = Ea - αEvib, where Ea is the activation energy for the thermal reaction, Evib is the vibrational energy of two colliding HI molecules, and α is estimated to be about 0.7. This means that a part of the vibrational energy of reacting HI is employed to reduce the activation energy for the translational or rotational degree of freedom.
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