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  • Physical Chemistry  (593)
  • Wiley-Blackwell  (593)
  • 1980-1984  (593)
  • 1925-1929
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 897-911 
    ISSN: 0538-8066
    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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  • 2
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    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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  • 3
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 4
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 603-613 
    ISSN: 0538-8066
    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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  • 5
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis resonance fluorescence technique has been used to reinvestigate the kinetics of the oxygen atom-oxygen molecule combination reaction. Third-order rate constants for O2, N2, and Ar as deactivant molecules were determined over the temperature range of 219-368 K. The results presented herein are the most extensive data sets available for atmospheric modeling and are used to formulate a recommendation for such purposes. The recommended rate expressions are \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1^{{\rm air}} = (1.07 \times 10^{ - 34})\exp (525/T){\rm cm}^{\rm 6} /{\rm molecule}^{\rm 2} {\rm sec} $$\end{document} or \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1^{{\rm air}} = (6.3 \times 10^{ - 34})\exp (T/300)^{\rm - 1.9}{\rm cm}^{\rm 6} /{\rm molecule}^{\rm 2} {\rm sec} $$\end{document} Comparisons of these results with existing literature data are presented.
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  • 6
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 7
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 555-568 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the pyrolysis of pyridine was studied in the temperature range of 875-1050°C, at 1 atm total pressure, in a Vycor stirred-flow reactor. Initial concentrations ranged from 0.25 to 2 mol % in helium and reaction times from 0.25 to 4 sec. It was found at the lower temperatures that the reaction was mixed first and second order. At the higher temperatures an autocatalytic term, zero order in the substrate and first order in the concentration of pyridine decomposed, was necessary in addition to the other two terms to describe the kinetic data. Most of the product was in the form of a primarily aromatic, nonvolatile tar; the major volatile products were HCN and C2H2. An increase in the surface-to-volume ratio of the reactor decreased the rate, indicating a radical chain or sequential reaction with radical consumption on the surface. Experiments with additives showed that C2H2 increased the rate. Using the kinetic and product data, some mechanistic considerations are discussed, and a mechanism is proposed to account for the first-order term.
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  • 8
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 9
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 303-316 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of the reverse reaction of the system has been measured in the range of 584-604 K from a study of the azomethane sensitized pyrolysis of isobutane. Assuming the published value for the rate constant of recombination of t-butyl we obtain \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k_{{\rm - 1}} (\sec ^{- 1}) = 14.67 - 39.4\,{\rm kcal}/{\rm mol}/(2.3{\rm RT}) $$\end{document} Combination with our published data for k1 permits the evaluation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log K_1 ({\rm atm}^{ - 1}) = 7.94\,\,{\rm at}\,\,600{\rm K} $$\end{document}We have modified a previously published structural model of t-butyl by the inclusion of a barrier to free rotation of the methyl groups in order to calculate values of the entropy and enthalpy of t-butyl as a function of temperature. Using standard data for H and for i-C4H8 we obtain \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta H_ f^\circ(t - {\rm butyl},\,300\,{\rm K})({\rm kcal}/{\rm mol}) = 10.6 \pm 0.5 $$\end{document}We have obtained other, independent values of this quantity by a reworking of published data using our new calculations of the entropy and enthalpy of t-butyl. There is substantial agreement between the different values with one exception, namely, that derived from published data on the equilibrium \documentclass{article}\pagestyle{empty}\begin{document}$$ i - {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} + {\rm I}\rightleftharpoons t{-} {\rm C}_4 {\rm H}_9 + {\rm HI} $$\end{document} which is significantly lower than the other values.We conclude that the value \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta H_ f^\circ(t - {\rm butyl},\,300\,{\rm K})({\rm kcal}/{\rm mol}) = 10.5 \pm 1.0 $$\end{document}obtained from the present work and a reworking of published data which involves the use of experimental data on t-butyl recombination is incompatible with the result based on iodination data.
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  • 10
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 637-647 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown how electron spin resonance spectroscopy with modulated radical initiation can be used to analyze by purely spectroscopic means the second-order termination kinetics of systems containing two different kinds of radicals. The technique is applied to species generated by photoreduction of acetone in tetraethoxy silane. The bimolecular self- and cross reactions of \documentclass{article}\pagestyle{empty}\begin{document}${\rm (CH}_{\rm 3} {\rm CH}_{\rm 2} {\rm O)}_{\rm 3} {\rm SiO\dot CHCH}_{\rm 3} (\dot R_1 )\,and\,(CH_3 )_2 \dot COH(\dot R_2 )$\end{document} are found to be encounter-controlled processes. For the cross termination the often used relation k12 = (4 k1k2)1/2 is verified experimentally.
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  • 11
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    International Journal of Chemical Kinetics 13 (1981), S. 411-416 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The entropy of activation for the hydrolysis of pentaphenoxyphosphorane in 25% aqueous dioxane is -188 J/mol deg. The enthalpy of activation is 22.5 kJ/mol, which is small for the relatively slow reaction. This suggests that the reaction is a multistep process having a preliminary equilibrium with a negative heat of reaction. This conclusion is supported by the results obtained for the hydrolysis of C6H5[OCH(CF3)2]2. A kinetic isotope effect kH2O/kD2O of 3.46 was found for the latter reaction. Orders in water were obtained, and a mechanism of hydrolysis is proposed.
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  • 12
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    International Journal of Chemical Kinetics 12 (1980), S. 699-716 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of di-tert-butyl sulfide has been investigated in static and stirred-flow systems at subambient pressures. The rate of consumption of the sulfide was measured in some experiments, and the rate of pressure increase was followed in others. The results suggest that the reaction is essentially homogeneous in a seasoned reactor and proceeds through a free radical mechanism. In the initial stages, the decomposition rate follows first-order kinetics, and the rate coefficient in the absence of an inhibitor is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{^u} (\sec ^{ - 1}) = 10^{15.1 \pm 0.6} \exp \left[{\left({ - 229 \pm 8} \right){\rm kJ/mol/RT}} \right] $$\end{document} between 360 and 413°C. The stoichiometry of the uninhibited reaction at 380°C and 50% decomposition is approximately \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm t}^{\rm \_} {\rm C}_{\rm 4} {\rm H}_{{\rm 9}^{\rm -}} {\rm S}_{\rm -} {\rm t}_{\rm -} {\rm C}_{\rm 4} {\rm H}_{\rm 9} = 1.72i_ - {\rm C}_{\rm 4} {\rm H}_{\rm 8} + 0.88{\rm H}_{\rm 2} {\rm S} + 0.29i_ - {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} + 0.11t_ - {\rm C}_{\rm 4} {\rm H}_{\rm 9} {\rm SH} $$\end{document} between 360 and 413°C. The stoichiometry of the uninhibited reaction at 380°C and 50% decomposition is approximately.
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  • 13
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    International Journal of Chemical Kinetics 12 (1980), S. 741-753 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The production of both the b1Σ+ and a1Δ states of NCl has been observed from the reaction of HN3 with flowing streams of Cl and F atoms. The results suggest that a two-step reaction sequence is responsible for the production of excited NCl, as follows: The rate contant (all products) for the first step is k(F + HN3) 〉 1 × 10-11 cm3/molecule sec. Comparison of this value to results obtained in a previous study of the F + HN3 system yields a value k(F + N3) = 2 × 10-12 cm3/molecule sec. The rate constant for the reaction of chlorine atoms with HN3 was determined to be k(Cl + HN3) 1 × 10-12 cm3/molecule sec. The difference between the Cl + HN3 and F + HN3 rates is interpreted in terms of an addition-elimination mechanism.
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  • 14
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    International Journal of Chemical Kinetics 12 (1980), S. 767-769 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 15
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    International Journal of Chemical Kinetics 12 (1980), S. 771-775 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 16
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    International Journal of Chemical Kinetics 12 (1980), S. 837-850 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of bromination of several aromatic compounds (anilides, anisoles, and phenols) was investigated in 80% aqueous acetic acid (v/v) in the temperature range 20-50°C using N-bromosuccinimide (NBS) as the reagent. The reaction was found to be first order in the aromatic substrate (ArH), and zero order in NBS, the overall order being 1. Stoichiometry of the reaction was 1:1. An increase in solvent polarity increased the reaction rate, and chloride ions were found to be specific catalysts for the reaction. Arrhenius activation energy remained almost constant for all the substrates. A probable mechanism explaining all these observed facts was proposed. The mechanism involved an attack by Br+ or more probably by a solvated Br+ ion on the aromatic substrate.
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  • 17
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 18
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photooxidation of the 1,3-butadiene-NO-air system at 298 ± 2 K was investigated in an environmental chamber under simulated atmospheric conditions. The irradiation gave rise to the formation of acrolein in a 55% yield, based on 1,3-butadiene initial concentration for all the experimental runs.The rate of formation of acrolein was the same as that of 1,3-butadiene consumption, indicating that acrolein is the major product of the 1,3-butadiene oxidation in air.The dependence of acrolein concentration on irradiation time showed thata secondary process, identified as an oxidation of acrolein by ⋅OH radicals, was occurring during the photochemical runs. The rate constant of this secondary process was determined by measuring the relative rates of disappearance of acrolein and n-butane during the irradiation of acrolein-n-butane-NO-air mixtures. The so obtained relative rate constant value was placed on an absolute basis using a reported rate constant for the n-butane + ⋅OH reaction; a value of (1.6 ± 0.2) × 1010 M-1 sec-1 was obtained.
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  • 19
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    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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  • 20
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 21
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    International Journal of Chemical Kinetics 13 (1981), S. 1125-1131 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a crossed laser-molecular beam study of nitromethane it was found that the excitation of nitromethane at 266 nm did not yield dissociation products under collision-free conditions. When a small cluster of nitromethane was excited at the same frequency, the product was seen only at energies and masses consistent with the rupture of the van der Waals bond by vibrational predissociation of the excited state.
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  • 22
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    International Journal of Chemical Kinetics 13 (1981), S. 1107-1123 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,1-Dichlorocyclopropane has been produced by addition of CH2(1A1) to 1,1-dichloroethylene. CH2(1A1) was generated by the photolysis of ketene at 277-334 nm. The 1,1-dichlorocyclopropane was formed in a chemically activated state, had an energy content between 386 and 400 kJ/mol, and reacted in two parallel channels to 2,3-dichloropropene and 1,1-dichloropropene. 1,1-Dichloropropene was also formed directly by insertion of CH2(1A1) into the CH bond of 1,1-dichloroethylene. As secondary reactions elimination of HCl from chemically activated 2,3-dichloropropene occurred with 3-chloropropyne and chloroallene as products. In some of the experiments perfluoropropane was added as an inert gas. The apparent rate constants for the isomerization and elimination reactions are reported. The results of RRKM calculations including distribution functions for the activated 1,1-dichlorocyclopropane and a step-ladder model for the deactivation verify the proposed reaction scheme.
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  • 23
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    International Journal of Chemical Kinetics 13 (1981), S. 1133-1142 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the gas-phase reactions of O3 with the carbonyls acrolein, crotonaldehyde, methacrolein, methylvinylketone, 3-penten-2-one, 2-cyclohexen-1-one, acetaldehyde, and methylglyoxal have been determined at 296 ± 2 K. The rate constants ranged from 〈6 × 10-21 cm3 molecule-1 s-1 for acetaldehyde to 2.13 × 10-17 cm3 molecule-1 s-1 for 3-penten-2-one. The substituent effects of —CHO and CH3CO— groups on the rate constants are assessed and discussed, as are implications for the atmospheric chemistry of the natural hydrocarbon isoprene.
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  • 24
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    International Journal of Chemical Kinetics 13 (1981), S. 1143-1150 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic equations for the decay of the free radicals in polymeric solids are given for the following assumptions on which they are based: (1) two simultaneous first-order but physically separated decay reactions; (2) two simultaneous noninteracting second-order decay reactions; (3) combined simultaneous but intermingled first- and second-order decay reactions; (4) the same but for independent, i.e., not intermingled, first- and second-order decay reactions; (5) a second-order decay reaction in the presence of some free radicals that do not decay; and (6) a first-order decay reaction in the presence of some free radicals that do not decay. In all of the above physical systems the total concentration only can be measured. Hence the above kinetic equations refer to the change of the total concentration with time. It is found that the data for the decay of the free radicals in irradiated isotactic polypropylene and 61% styrene-39% butadiene block copolymer agree best with the equations for the second-order decay in the presence of a fraction of nondecaying free radicals.
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  • 25
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    International Journal of Chemical Kinetics 13 (1981), S. 69-84 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of O(3P) atoms with propanehas been studied at temperatures near 300 K by using a discharge flow system. Oxygen atoms were generated in the absence of molecular oxygen by the reaction N + NO → N2 + O, nitrogen atoms having been generated in a microwave discharge. Rate constants for the reaction were measured in two ways, either by measurement of O-atom decay in the presence of excess propane or by measuring the change in propane concentration after an appropriate time in the presence of an excess of oxygen atoms. The two methods were in good agreement, and the mean rate constant at 306 K is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = (4.7 \pm 0.8) \times 10^6 {\rm dm}^3 /{\rm mol}\;\sec $$\end{document} A study of the products of the reaction under conditions corresponding to complete removal of oxygen atoms has shown that an important product of the reaction in the early stages is propene. This is difficult to explain interms of a mechanism involving alkoxy radicals similar to that which has been proposed for some other O(3P)-hydrocarbon reactions. An alternative mechanism is proposed in terms of successive hydrogen abstraction reactions.
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  • 26
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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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  • 27
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    International Journal of Chemical Kinetics 13 (1981), S. 135-148 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of the cerium (IV) oxidation of p-chloromandelic acid has been studied in perchlorate media at an ionic strength of 1.50 mol/dm3 by the stopped-flow technique and in H2SO4—MHSO4 (M+ = Li+, Na+, K+) and H2SO4—MClO4 (M+ = H+, Li+, Na+) mixtures at constant total electrolyte concentrations of 1.00 and 2.00 mol/dm3 using the conventional spectrophotometric method. In perchlorate media the kinetic data indicate the formation of two intermediate complexes between cerium (IV) and the organic substrate, but only one is significantly involved in the intramolecular electron-transfer process. The oxidation rate is markedly lower in sulfate media, where two reaction paths have been found to contribute to the overall redox reaction. The univalent cations examined exhibit negative specific effects upon the overall oxidation rate increasing in the order H+ 〈 Li+ 〈 Na+ 〈 K+. Activation parameters have been also estimated.
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  • 28
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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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    International Journal of Chemical Kinetics 13 (1981), S. 209-217 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By measuring the rates of decay of ozone in a large excess of reactant, second-order rate constants have been obtained for the reactions of ozone with ethene, propene, but-1-ene, trans-but-2-ene, isobutene, hex-1-ene, cyclopentene, cyclohexene, isoprene, vinyl fluoride, 1,1-difluoroethene, cis-1,2-difluoroethene, trans-1,2-difluoroethene, trifluoroethene, tetrafluoroethene, and 2,5—dihydrofuran. The reactions have been studied in synthetic air at atmospheric pressure and at temperatures of 294 and 260 K. The rate constants and Arrhenius parameters are discussed in relation to existing kinetic data on ozone-alkene reactions.
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  • 30
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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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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    International Journal of Chemical Kinetics 13 (1981), S. 333-365 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Models for the energy profile along the reaction coordinate are utilized to determine the barrier's height and location as a function of ΔG. These form the basis for structure-reactivity correlations and afford a unified formulation for various postulates in the field of physical organic chemistry. Current experimental evidence is examined for the resulting correlations, and some of their applications as an aid to the chemical kineticist are presented.
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    International Journal of Chemical Kinetics 13 (1981), S. 403-410 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of pyrolysis of 4-chloro-2-butanone in the gas phase have been determined in a static system seasoned with the products of decomposition of allyl bromide. The reaction is catalyzed by hydrogen chloride. Under maximum catalysis of HCl, the kinetics were found to be of order 1.5 in the substrate suggesting that a complex elimination is involved. The reaction, when maximally inhibited with propene, appears to undergo a unimolecular elimination and follows a first-order law kinetics. The products are methylvinyl ketone and hydrogen chloride. The kinetics have been measured over the temperature range of 402.0-424.4°C.The rate coefficients are given by the Arrhenius equation \documentclass{article}\pagestyle{empty}\begin{document}$ \log k_1 (\sec ^{ - 1}) = (13.67 \pm 0.69) - (225.2 \pm 8.6)\,{\rm kj}/{\rm mol}/2.303RT\angle $\end{document}. Thepyrolysis of 4-chloro-2-butanone is 31 times greater in rate than that of ethyl chloride at 440°C. This large difference in rate may be attributed to the -M effect of the acetyl substituent in the pyrolysis of the former halo compound.
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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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    International Journal of Chemical Kinetics 13 (1981), S. 445-462 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal unimolecular decomposition of ethylbenzene, isopropylbenzene, and tert-butylbenzene was studied using the very-low-pressure pyrolysis (VLPP) technique. Each reactant decomposed by way of β C—C bond homolysis, producing methyl radicals and benzyl or benzylic-type radicals. RRKM calculations show that the observed rate constants, when combined with thermochemical estimates, are consistent with the following high-pressure rate expressions: \documentclass{article}\pagestyle{empty}\begin{document}$ \log k(\sec ^{ - 1}) = 15.3 - (72.7/{\rm \theta)} $\end{document} for ethylbenzene between 1053 and 1234 K, \documentclass{article}\pagestyle{empty}\begin{document}$ \log k(\sec ^{ - 1}) = 15.8 - (71.3/{\rm \theta)} $\end{document} for isopropylbenzene between 971 and 1151 K, and \documentclass{article}\pagestyle{empty}\begin{document}$ \log k(\sec ^{ - 1}) = 15.9 - (69.1/{\rm \theta)} $\end{document} for tert-butylbenzene between 929 and 1157 K, where θ (kcal/mol) = 2.303RT. Resulting activation energies combined with heat capacity and heat of formation data led to the following dissociation enthalpies and enthalpies of formation at 298 K: DH° (øCH(CH3)—CH3) = 73.8 kcal/mol, ΔHf° (øÇCH(CH3)) = 39.6 kcal/mol, DH° (øC(CH3)2—CH3) = 72.9 kcal/mol, and ΔHf° (øÇ(CH3)2) = 32.4 kcal/mol. Derived high-pressure rate constants are in good accord with results of lower temperature toluene- and aniline-carrier experiments.
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    International Journal of Chemical Kinetics 13 (1981), S. 481-495 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of ethane has been reinvestigated using the single pulse, reflected shock technique. Reflected shock temperatures were corrected for boundary layer-induced nonidealities using the thermal decomposition of cyclohexene as a kinetic standard. The rate constant for the reaction was calculated from the rate of formation of methane under conditions of very low extent of reaction, over a temperature range of 1000-1241 K. Ethane compositions of 1% and 3% in argon at total reaction pressures of 3 and 9 atm were used, and a small pressure dependence of k1 was observed.An RRKM model is described which gives excellent agreement with this and other recent dissociation and recombination rate constant data in light of a recent revision to the thermochemistry of the methyl radical. In the range of 1000-1300 K an RRKM extrapolated k1∞ is given by the expression, log k1∞ = 17.2 - 91,000/2.3RT, while at 298 K the calculation gives log k-1∞ (l/mol sec) = 10.44, where k-1∞ is calculated from k1∞ and the equilibrium constant.
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    International Journal of Chemical Kinetics 13 (1981), S. 1297-1301 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that chain reactions may be studied in stirred-flow reactors under conditions in which the escape of radicals from the reactor competes significantly with the chemical termination reaction. The appropriate rate law permits the independent evaluation of the rate constants of the initiation and termination steps. Such information is of special interest in the study of surface effects on chain reactions.
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    International Journal of Chemical Kinetics 13 (1981), S. 1277-1288 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: According to our experiments the bromide ion concentration exhibits in the bromate-ascorbic acid-malonic acid-perchloric acid system three extrema as a function of time. To describe this peculiar phenomenon, the kinetics of four component reactions have been studied separately. The following rate equations were obtained:Bromate-ascorbic acid reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} { - d[{\rm BrO}_3^ -]/dt = k_1 [{\rm BrO}_3][{\rm H}_2 {\rm A],}} & {k_1 = 8.3 \times 10^{ - 3} M^{ - 1} \cdot {\rm s}^{ - {\rm 1}} } \\ \end{array} $$\end{document}Bromate-bromide ion reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} { - d[{\rm BrO}_3^ -]/dt = k_2 [{\rm BrO}_3][{\rm Br}^ -][{\rm H}^ +]^2,} & {k_2 = 3.6M^{ - 3} \cdot {\rm s}^{ - 1} } \\ \end{array} $$\end{document}Bromide-ascorbic acid reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} { - d[{\rm Br}_{\rm 2}]/dt = k_3 [{\rm Br}_2][{\rm H}_2 {\rm A],}} & {k_3 \ge 1.7 \times 10^{ - 3} \cdot {\rm s}^{ - 1} } \\ \end{array} $$\end{document}Bromine-malonic acid reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} { - d[{\rm Br}_{\rm 2}]/dt = k_4 k_4 [{\rm Br}_2][{\rm H}_2 {\rm M}]/(k_4 + k_5 [{\rm Br}_2]),} & {k_4 = 6 \times 10^{ - 3} {\rm s}^{ - 1} } \\ \end{array}, \quad {\rm }k_{ - 4} \ge 1.7 \times 10^{ - 3} \cdot {\rm s}^{ - 1} \quad {\rm }k_5 \ge 1 \times 10^7 M^{ - 1} \cdot {\rm s}^{ - 1} $$\end{document} k4 = 6 × 10-3 s-1, k-4 ≥ 1.7 × 103 s-1, k5 ≥ 1 × 107M-1 · s-1Taking into account the stoichiometry of the component reactions and using these rate equations, the concentration versus time curves of the composite system were calculated. Although the agreement is not as good as in the case of the component reactions, it is remarkable that this kinetic structure exhibits the three extrema found.
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    International Journal of Chemical Kinetics 13 (1981), S. 1303-1303 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    International Journal of Chemical Kinetics 14 (1982) 
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    Keywords: Chemistry ; Physical Chemistry
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    International Journal of Chemical Kinetics 14 (1982), S. 1-12 
    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 NH2 radicals with ethyl, isopropyl, and t-butyl radicals have been measured at 298 K, using a flash photolysis-laser resonance absorption method. Radicals were generated by flashing ammonia in the presence of an olefin. A new measurement of the NH2 extinction coefficient and oscillator strength at 597.73 nm was performed. The decay curves were simulated by adjusting the rate constants of both the reaction of NH2 with the alkyl radical and the mutual interactions of alkyl radicals. The results are k(NH2 + alkyl) = 2.5 (±0.5), 2.0 (±0.4), and 2.5 (±0.5) × 1010 M-1·s-1 for ethyl, isopropyl, and t-butyl radicals, respectively. The best simulations were obtained when taking k(alkyl + alkyl) = 1.2, 0.6, and 0.65 × 1010M-1·s-1 for ethyl, isopropyl, and t-butyl radicals, respectively, in good agreement with literature values.
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    International Journal of Chemical Kinetics 13 (1981), S. 627-638 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(trifluoromethyl) peroxide is readily dissociated by multiple infrared photon excitation at CO2 laser wavelengths. The primary dissociation product is CF3O; approximately 85% of the nascent radicals are further dissociated in the laser field to form CF2O and F. The F atoms then react with the remaining CF3O to produce CF3OF. The formation of CF3OF is strongly inhibited by addition of HI, which reacts preferentially with the F atoms.
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    International Journal of Chemical Kinetics 13 (1981), S. 667-675 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constant for the reaction of methyl radicals with ozone has been measured as a function of temperature. Small concentrations of CH3 were generated by flash photolyzing CH3NO2 at 193 nm with an ArF laser. A photoionization mass spectrometer was used to follow the rate of decay of CH3 at various ozone concentrations. The resulting rate constants could be fit by the expressions \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = (5.4 \pm 1.5) \times 10^{ - 12} \exp [(- 216 \pm 80)/T]{\rm cm}^3 /{\rm molec}\,{\rm s} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = (2.6 \pm 0.7) \times 10^{ - 12} {\rm (T/300)}^{{\rm 0}{\rm .71} \pm {\rm 0}{\rm .34}} {\rm cm}^3 /{\rm molec}\,{\rm s} $$\end{document} over the temperature range of 243-384 K. These rate constants can be modeled by simple transition state theory using reasonable parameters for the activated complex. Use of this rate constant shows that less than 1% of the methyl radicals formed in the stratosphere react with ozone.
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    International Journal of Chemical Kinetics 13 (1981) 
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    Keywords: Chemistry ; Physical Chemistry
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    International Journal of Chemical Kinetics 13 (1981), S. 707-728 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction C2H5 + O2 → C2H5O2 in glassy methanol-d4 and the H-atom abstraction by CH3, C2H5, and n-C4H9 radicals in C2H5OH + C2D5OH and CD3CH2OH + C2D5OH glassy mixtures have been studied by electron spin resonance. The analysis of the dependence of the reaction rates on the concentration of O2 (oxidation) and C2H5OH, CD3CH2OH (H-atom abstraction) has shown that the √t law is not conditioned by the existence of regions characterized by different rate constants.
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    International Journal of Chemical Kinetics 14 (1982), S. 35-42 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis of biacetyl produces CO, C2H6, and CH3COCH3 as main products, and in small amounts CO2, C2H4, and CH3CHO. The rate constants of reactions (2) and (3) \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {(1)} {2{\rm CH}_3 \to {\rm C}_2 } \\ \end{array}{\rm H}_6 $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {(2)} {{\rm CH}_3 + {\rm CH}_3 {\rm CO} \to {\rm CH}_3 {\rm COCH}_3 } \\ \end{array} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {(3)} {2{\rm CH}_3 {\rm CO} \to {\rm CH}_3 {\rm COCOCH}_3 } \\ \end{array} $$\end{document} of thermally equilibrated radicals were calculated from the amounts of products: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k_2 = (2.98 \pm 0.17){\rm 10}^{{\rm 10}} {\rm dm}^{\rm 3} /{\rm mol} \cdot {\rm s} \\ k_3 = (2.43 \pm 0.14){\rm 10}^{{\rm 10}} {\rm dm}^{\rm 3} /{\rm mol} \cdot {\rm s} \\ \end{array} $$\end{document}.
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    International Journal of Chemical Kinetics 13 (1981), S. 799-815 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: H atoms react with C2H5SSC2H5 to give C2H5SH as the sole retrievable product with φ = 2.32 at 25°C and 2.84 at 145°C. The primary reaction is postulated to be H + C2H5SSC2H5 ← C2H5SH + C2H5S with k1 = (4.73 ± 0.64) × 1013 exp [-(1710 ± 69)/RT] cm3/mol·s relative to the rate constant of the H + C2H4 ← C2H5 reaction. The high value of the entropy of activation suggests the presence of partial hydrogen bonding in diethyldisulfide which is broken in the transition state.Ethylmethyldisulfide reacts similarly: H + C2H5SSCH3 ← C2H5SH + CH3S or CH3SH + C2H5S. The thiyl radicals propagate a chain of radical exchange reactions forming the symmetrical disulfides with exposure-time-dependent quantum yields. The overall kinetics conform to a 16-step mechanism from which the rate constants of the elementary reactions could be established by computer modeling. Thiyl radicals react considerably more slowly with disulfides than H atoms.
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mesityl 2,6-xylyl ketone in 89.8% (w/w) sulfuric acid undergoes cleavage to give mesitylenesulfonic acid, xylenesulfonic acid, and carbon dioxide as final products. The reaction has been analyzed in terms of a series of first-order reactions. Of the two possible reaction paths available it was shown that fission at the mesityl group is responsible for about 98.5% of the overall initial reaction at 25°C.
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    Keywords: Chemistry ; Physical Chemistry
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    International Journal of Chemical Kinetics 13 (1981), S. 873-881 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: CFBr radicals produced by the reaction of atomic oxygen with F2CCFBr were monitored in a discharge flow system by fluorescence excited at 424 nm. The rate coefficients for reactions of the CFBr radicals were measured between 298 and 358 K, and the following values were obtained in units of cm3/molec·s: O2 〈 2 × 10-16 at 353 K; NO 〈 10-14 at 298 K; F2CCFBr 〈 10-15 at 298 K; Cl2 (1.9 ± 0.6) × 10-12 exp(-762 ± 92/T) Br2 (1.4 ± 0.3) × 10-12 exp(-533 ± 62/T).
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    International Journal of Chemical Kinetics 14 (1982), S. 447-450 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    International Journal of Chemical Kinetics 14 (1982), S. 565-583 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results are reported from moderated nuclear recoil 18F experiments with the 273 K CHF3/C3F6/C2F6 system. Although the measurement sensitivity is only about ±12%, there is no evidence to support the occurrence of nonthermal F-to-HF reactions at 95 mol % C2F6 moderator concentration.
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    International Journal of Chemical Kinetics 14 (1982), S. 543-564 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The main difference between the simple RRK theory and the better based but more complex RRKM theory is explained. Starting from the premise that the classical versus quantum mechanical estimation of the density of states is the major source of the difference, earlier attempts to incorporate the quantum effects in an effective value for the number of oscillators s are noted. By examining the expression for the RRKM rate coefficient it is found that a single effective s value will generally not suffice, but a much better representation of the quantum effects can be obtained if it is recognized that the problem inherently contains two different effective s values. A theory based on this analysis is constructed. It reproduces RRKM results to much improved accuracy, removing difficulties found earlier with single-s-value theories.
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  • 55
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An iterative method has been devised for the simulation of chemiluminescence data during the oxidative decomposition of αα′ azobisisobutyronitrile in the presence of ethylbenzene. From this simulation the cross termination rate constant of the two types of peroxy radicals present has been estimated.
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  • 56
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    International Journal of Chemical Kinetics 14 (1982), S. 659-668 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of gamma-radiation-induced free-radical reactions in carbon tetrachloride solutions of ethanol and n-pentanol were studied in the range of 0.05-0.80M and 25-170°C. The rate constant for the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CCl}_{\rm 3} + {\rm R} - CH_2 - {\rm OH}\mathop \to \limits^{k1} {\rm CHCl}_{\rm 3} + {\rm R} - {\rm CH} - {\rm OH}$$\end{document} was found as \documentclass{article}\pagestyle{empty}\begin{document}$$k1(M^{- 1} \cdot s^{- 1}) = 10^{8.6 \pm 0.4} \exp - (\frac{{9900 \pm 600{\rm cal}}}{{RT}})$$\end{document} The activation energy is larger by 0.8 kcal/mol than for secondary alcohols, while the A1 factors are about the same.
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  • 57
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    International Journal of Chemical Kinetics 14 (1982), S. 647-657 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the gas-phase thermal reaction between CF2(OF)2 and CO has been studied in a static system at temperatures ranging between 110 and 140°C. The only reaction products were CF2O and CO2, giving the following stoichiometry: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CF}_{\rm 2} {\rm (OF)}_{\rm 2} {\rm + 2CO = 2CF}_{\rm 2} {\rm O + CO}_{\rm 2} {\rm}\Delta n{\rm = 0}$$\end{document} The reaction is homogeneous. The rate is strictly second order in CF2(OF)2 and CO, and is not affected by the total pressure or by the presence of reaction products. Oxygen promotes a sensitized oxidation of CO and inhibits the formation of CF2O.The experimental results in the absence of oxygen can be explained by a chain mechanism similar to that proposed for the reaction between F2O and CO with an overall rate constant of \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = 1.45 \times 10^9 {\rm exp}(- 20,900/RT)L/mol \cdot s$$\end{document} From the experimental data obtained on the oxygen-inhibited reaction, the rate constant for the primary process can be calculated: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {({\rm I})} \quad {{\rm CF}_{\rm 2} ({\rm OF)}_{\rm 2} + {\rm CO} \to {\rm CF}_{\rm 2} (\mathop {\rm O}\limits^{\rm .}){\rm OF} + {\rm F}\mathop {\rm C}\limits^{\rm .} {\rm O}} \quad\quad {k_1 = 1.45 \times 10^9 {\rm exp}(- 20,900/RT)L/mol \cdot s} \\\end{array}$$\end{document} The chain length v = 2.5 is independent of the temperature. Taking for collision diameters σCF2(OF)2 = 6 Å and σCO = 3.74 Å, a value α = 5.3 × 10-3 for the steric factor is obtained.
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    International Journal of Chemical Kinetics 14 (1982), S. 679-697 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A nozzle-beam-skimmer sampling system is used to measure species concentration profiles for a lean one-dimensional premixed CO—O2—Ar flame, into which small amounts of sulfur dioxide are introduced. The net formation rate for sulfur trioxide is obtained from the flux fraction profile for this species. The kinetic scheme is then utilized, along with the measured temperature profiles, to evaluate the rate coefficients k1 and k2 over the temperature range of 1435-1850 K. The most satisfactory agreement between the measured net formation rate for SO3 and that calculated on the basis of reactions (1) and (2) is obtained with the rate coefficients \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = 4.4 \times 10^{14} \exp [3163/T]{\rm cm}^{\rm 6} {\rm /mol}^{\rm 2} \cdot {\rm s}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_2 = 1.32 \times 10^{12} \exp [- 3070/T]{\rm cm}^{\rm 3} {\rm /mol} \cdot {\rm s}$$\end{document} Reactions (1) and (2) are found to be nearly balanced in a substantial region of the flame. Here the data are more sensitive to the difference in activation energies, as opposed to a particular value for either. Implications of this observation on the uncertainty of the deduced temperature dependence for each reaction are discussed, as are some of the procedures used in the data analysis.
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  • 59
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    International Journal of Chemical Kinetics 14 (1982), S. 669-677 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title reaction has been investigated in the temperature range of 490-573 K. Initial reactant pressures were varied in the range of 0.2-5.2 torr (I2) and 2-20 torr (C6H5SiH3). The rate of iodine consumption, monitored spectrophotometrically, was found to obey \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm I}_{\rm 2}]}}{{dt}} = \frac{{k_{3/2} [{\rm I}_{\rm 2}]^{{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$2$}}} [{\rm C}_{\rm 6} {\rm H}_{\rm 5} {\rm SiH}_{\rm 3}]}}{{1 + k'[HI]/[I_2]}}$$\end{document} both by initial rate and integrated equation fitting procedures. The effect of added initial HI conformed to this expression. The data are consistent with a conventional I-atom propagated chain reaction, and for the step \documentclass{article}\pagestyle{empty}\begin{document}$${\rm I}^{\rm .} + {\rm C}_{\rm 6} {\rm H}_{\rm 5} {\rm SiH}_{\rm 3} \to {\rm C}_{\rm 6} {\rm H}_{\rm 5} \mathop {\rm S}\limits^{\rm .} {\rm iH}_{\rm 2} + {\rm HI}$$\end{document} the rate constant is given by \documentclass{article}\pagestyle{empty}\begin{document}$${\rm log}k_1 (dm^3 /mol \cdot s) = (11.52 \pm 0.08) - (76.8 \pm 0.8{\rm kJ/mol})/RT{\rm ln}10$$\end{document} From this is derived the bond dissociation energy value C6H5SiH2—H = 374 kJ/mol(88 kcal/mol). A comparison with other Si—H dissociation energy values indicates that the “silabenzyl” stabilization energy is small, ≈7 kJ/mol.
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    International Journal of Chemical Kinetics 14 (1982) 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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    International Journal of Chemical Kinetics 14 (1982), S. 733-733 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
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  • 62
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    International Journal of Chemical Kinetics 14 (1982), S. 801-811 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic study on the oxidation of V(IV) by chloramine-T (CAT) at pH 6.85 by N-bromo succinimide (NBS) in aqueous acetic acid-perchloric acid media and by N-iodo succinimide (NIS) in aqueous perchloric acid medium has been carried out. In all the systems studied the order with respect to the oxidant is unity. NBS and CAT oxidation reactions exhibited Michaelis-Menten type kinetics, and the NIS study indicated unit dependence on [substrate]. Independence on acidity has been observed in the case of CAT and NBS reactions, but NIS reactions exhibited inverse unit dependence on [acid]. Novel solvent influences have been noticed in the case of CAT reactions, but with NIS and NBS reactions retardation in the rate has been observed with an increase in the percentage of acetic acid. Plausible mechanisms consistent with the results have been postulated, and suitable rate laws in consonance with the postulated mechanisms have been derived.
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    International Journal of Chemical Kinetics 14 (1982), S. 813-814 
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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 14 (1982), S. 815-821 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The experimental behavior of the cerium- and manganese-catalyzed Belousov Zhabotinskii oscillating reaction with ethyl acetoacetate as organic substrate has been investigated. Under certain conditions the system displays two types of temporal oscillations. Damped highfrequency oscillations appear immediately after the addition of potassium bromate solution to complete the reaction mixture. These high-frequency oscillations may be regarded as being superimposed on an induction period of the type found in the reaction using malonic acid. After the induction period, low-frequency oscillations of the normal type are obtained. Both the high-frequency and the low-frequency oscillations can be monitored with a platinum redox or with a bromide specific ion electrode.
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  • 65
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic spectrophotometric investigation of the reaction of the hydrogen peroxide anion with methyl p-nitrophenyl sulfate in methanol solvent resulted in the evaluation of the pKa of HOOH in methanol at 25°C as 15.8 ± 0.2. Since normal kinetic procedures for the determination of the equilibrium constant K for the process CH3O- + H2O2 ⇄ CH3OH + HO2- were found to be associated with high uncertainty, another procedure was devised to establish the magnitude of K. This method is based on an analysis of the changing slopes of plots of pseudo-first-order rate constants against the total base concentration as the stoichiometric amount of hydrogen peroxide is varied. The method is applicable to any system in which anionic nucleophiles generated in situ compete with solvent anions. Such a corroboration of kinetically determined equilibrium constants is believed essential. The kinetic data allow the specific rate constant kHOO-for the reaction of methyl p-nitrophenyl sulfate with hydrogen peroxide anions to be evaluated and yield the rate constant ratio kHOO-/kMeO- = 8.8 ± 2.2. This confirms the existence of an α effect at saturated carbon in this system.
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    International Journal of Chemical Kinetics 14 (1982), S. 1139-1147 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of diphenyl sulfide with the two oxidants peroxydisulfate and peroxydiphosphate are described. With each oxidant, the reaction is first order in the oxidant and zero order in the substrate. The rate of the reaction is also independent of the effect of the substituent. Hydrogen ion catalyzes the reactions. The lack of inhibition of the reaction rate by added acrylamide rules out the possibility of a radical reaction initiated by the homolysis of the peroxyanions. From the effect of [H+] on the oxidation rates, the active species involved in the reactions have been determined. The redox reaction is essentially proceeding via hydrolysis of the protonated peroxy anions in a rate-determining step, followed by a fast step involving the oxidation of diphenyl sulfide to diphenyl sulfoxide. This has been confirmed by estimating the hydrolyzed products in each case and also by the product analyses.
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    International Journal of Chemical Kinetics 14 (1982), S. 1149-1161 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis resonance fluorescence technique has been used to measure the rate constant for the reaction over the temperature range of 250-370 K. The present results are in excellent agreement with three very recent studies, and the combined data set can been used to derive the expression similar to that currently used in atmospheric modeling applications.A summary of our computer simulation of this reaction system is presented. The results of the computations indicate the absence of secondary reaction complications in the present work while revealing significant problems in the earlier (pre-1980) studies of the title reaction.
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    International Journal of Chemical Kinetics 14 (1982), S. 1165-1182 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results are reported from moderated nuclear recoil 18F experiments with the CH4/C3F6/C2F6 mixture system. At a 99.5% confidence level measurement precision of ±3.4%, non-thermal F-to-HF reactions are phenomenologically suppressed at C2F6 moderator concentrations in the range of 95.0-99.95 mol-%. Effectively equilibrium reaction conditions can be established in well-designed experiments of this type.
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    International Journal of Chemical Kinetics 14 (1982), S. 1211-1218 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rates of oxidation of XCOO- (X = H, D) by Br2 in acid aqueous media were measured between 274 and 332 K. The derived Arrhenius parameters for both reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\log k_{\rm H} (M^{- 1} {\rm s}^{{\rm - 1}}) = (11.18 \pm 0.10) - (14.33 \pm 0.13)/\theta $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$\log k_{\rm D} (M^{- 1} {\rm s}^{{\rm - 1}}) = (13.77 \pm 0.13) - (17.62 \pm 0.04)/\theta $$\end{document} where θ = 4.575T × 10-3 kcal/mol, with (kH/kD)298K = 2.85, reveal a primary isotope effect, but the difference (ED - EH) = 3.29 kcal/mol and the ratio AD/AH = 91 fall beyond the limits imposed by semiclassical transition-state theory, suggesting tunneling or a multiple-stage mechanism. However, it can be shown that either tunneling in a single step or a three-step, internal return mechanism can be ruled out as alternative models, since both require unreasonable kinetic parameters to fit the data. The simplest scheme accounting for the present observations involves tunneling in the decomposition of a charge transfer complex in equilibrium with the reactants.
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    International Journal of Chemical Kinetics 14 (1982), S. 1183-1197 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of arginine, histidine, and threonine by chloramine-T (CAT) have been investigated in alkaline medium at 35°C. The rates are first order in both [CAT] and [amino acid] and inverse fractional order in [OH-] for arginine and histidine. The rate is independent of [OH-] for threonine. Variation of ionic strength and addition of the reaction product, p-toluenesulfonamide, or Cl- ions had no effect on the rate. A decrease of the dielectric constant of the medium by adding methanol decreased the rate with arginine, while the rates increased with histidine and threonine. The solvent isotope effect was studied using D2O. (kobs)D2O/(kobs)H2O was found to be 0.55 and 0.79 for arginine and histidine, respectively. The reactions were studied at different temperatures, and activation parameters have been computed. The oxidation process in alkaline medium, under conditions employed in the present investigations, has been shown to proceed via two paths, one involving the interaction of RNHCl (formed rapidly from RNCl-), with the amino acid in a slow step to form monochloroamino acid, which subsequently interacts with another molecule of RNHCl in a fast step to give the products, p-toluenesulfonamide (RNH2), and the corresponding nitrile of the amino acid (R'CN). The other path involves the interaction of RNCl- with the amino acid in a similar way to give RNH2 and R'CN. Mechanisms proposed and the derived rate laws are consistent with the observed kinetics. The rate constants predicted using the derived rate laws, as [OH-] varies, are in excellent agreement with the observed rate constants, thus justifying these rate laws and hence the proposed mechanistic schemes.
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    International Journal of Chemical Kinetics 15 (1983), S. 37-50 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative rate constants for the gas-phase reactions of OH radicals with a series of bi- and tricyclic alkanes have been determined at 299 ± 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 cyclohexane of 7.57 × 10-12 cm3/molec·s, the rate constants obtained are (× 1012 cm3/molec·s): bicyclo[2.2.1]heptane, 5.53 ± 0.15; bicyclo[2.2.2]octane, 14.8 ± 1.0; bicyclo[3.3.0]octane, 11.1 ± 0.6; cis-bicyclo[4.3.0]nonane, 17.3 ± 1.3; trans-bicyclo[4.3.0]nonane, 17.8 ± 1.3; cis-bicyclo[4.4.0]decane, 20.1 ± 1.4; trans-bicyclo[4.4.0]decane, 20.6 ± 1.2; tricyclo[5.2.1.02,6]decane, 11.4 ± 0.4; and tricyclo[3.3.1.13,7]decane, 23.2 ± 2.1. These data show that overall ring strain energies of ≲4-5 kcal mol-1 have no significant effect on the rate constants, but that larger ring strain results in the rate constants being decreased, relative to those expected for the strain-free molecules, by ratios which increase approximately exponentially with the overall ring strain.
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    International Journal of Chemical Kinetics 15 (1983), S. 51-61 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the reactions of O3 and OH radicals with furan and thiophene have been determined at 298 ± 2 K. The rate constants obtained for the O3 reactions were (2.42 ± 0.28) × 10-18 cm3/molec·s for furan and 〈6 ×10-20 cm3/molec·s for thiophene. The rate constants for the OH radical reactions, relative to a rate constant for the reaction of OH radicals with n-hexane of (5.70 ± 0.09) × 10-12 cm3/molec·s, were determined to be (4.01 ± 0.30) × 10-11 cm3/molec·s for furan and (9.58 ± 0.38) × 10-12 cm3/molec·s for thiophene. There are to date no reported rate constant data for the reactions of OH radicals with furan and thiophene or for the reaction of O3 with furan. The data are compared and discussed with respect to those for other alkenes, dialkenes, and heteroatom containing organics.
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    International Journal of Chemical Kinetics 15 (1983), S. 341-380 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using currently available thermochemical and kinetic data and estimation methods to analyze the thermochemistry and the kinetic parameters of the elementary reactions involved in the oxidation of HCl and HBr, reaction mechanisms are proposed which account for the previously reported reaction products, the rate law, and the kinetic data. For oxidation of HCl, two competitive pathways, the radical initiation by hydrogen abstraction and the fourcenter reaction pathway, were invoked to account for the observations. In the oxidation of HBr one must invoke a fast surface reaction of the type \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm H}_2 {\rm O}_2 + {\rm HBr}({\rm S}) \to 2{\rm H}_2 {\rm O} + {\rm Br}_2 ({\rm g}) $$\end{document} to account for the reaction.
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    Keywords: Chemistry ; Physical Chemistry
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    International Journal of Chemical Kinetics 15 (1983), S. 381-395 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This investigation of the kinetics and thermodynamics of the thermal isomerization reaction of 1α,25-dihydroxycholecalciferol, the physiologically active metabolite of vitamin D3, is based on the simultaneous determinations of 1α,25-(OH)2D3 and its previtamin analog by nuclear magnetic resonance spectroscopy which distinguishes these compounds from possible impurities. The kinetics at different temperatures are used to obtain the activation parameters for the sigmatropic [1,7] thermal interconversion process which is shown to be compatible with a reaction that is unimolecular and concerted. The nature of the transition state of the activated complex, the reaction energetics, and the relative stabilities of 1α,25-(OH)2D3 and vitamin D3 are discussed.
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    International Journal of Chemical Kinetics 15 (1983), S. 537-546 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reversible thermal gas-phase dimerization of hexafluoropropene to the four isomeric cyclobutanes has been studied by pressure change and by gas-liquid chromatographic analysis in the temperature range of 645-708 K with initial pressures of olefin from 802 to 4820 mm Hg. The reaction was accurately second order at low conversions of olefin to dimers, and at higher conversions it gave a very good fit to the rate equation for opposing second- and first-order reactions. The rate constants for the dimerization, calculated from initial rates of reaction, yielded the least-mean-squares Arrhenius equation (95% confidence limits): \documentclass{article}\pagestyle{empty}\begin{document}$$ \log _{10} (k_2 /{\rm dm}^3 {\rm mol}^{ - 1} s^{ - 1}) = (5.93 \pm 0.40) - (131.8 \pm 9.5)k{\rm J\,\,mol}^{{\rm - 1}}/RT\ln \,10 $$\end{document} where k2 is defined by \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{ - 1/2{\rm d}[{\rm C}_3 {\rm F}_6]}}{{dt}} = \frac{{{\rm d}[c - {\rm C}_6 {\rm F}_{12}]}}{{dt}} = k_2 [{\rm C}_3 {\rm F}_6]^2 $$\end{document} Studies carried out in a packed vessel showed no evidence of heterogeneity. The rate constants found in this work are in excellent agreement with those found at lower pressures by Atkinson and Tsiamis, and the combined results give the Arrhenius equation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log _{10} (k_2 /{\rm dm}^{\rm 3} {\rm mol}^{{\rm - 1}} {\rm s}^{{\rm - 1}}) = (6.47 \pm 0.21) - (138.6 \pm 2.7){\rm kJ\,mol}^{{\rm - 1}} {\rm /}RT\ln 10 $$\end{document}
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    International Journal of Chemical Kinetics 16 (1984), S. 397-405 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A vacuum ultraviolet photolysis of C2H5Br at 147 nm was studied over a pressure range of 0.5-50 torr at 298 K. The effects of additives He and NO were also investigated.The principal reaction products were found to be C2H4 and C2H6, with lesser yields of CH4 and C2H2. With increasing pressure the product quantum yields Φi of C2H4, CH4, and CH2H6 remained constant, while that of C2H2 decreased from 0.03 to almost 0. The effect of He as an additive was found to be extremely small on the quantum yields of the major products. Addition of NO completely suppresses the formation of CH4, C2H2, and C2H6, and reduces partially the production of C2H4. The primary processes appear to involve two electronically excited states. One state mainly yields C2H4 by molecular elimination of HBr and is thought to be due to a Rydberg transition. The other state decomposes to C2H5 and Br radicals by C—Br bond fission. These two competitive reaction modes contribute to the photodecomposition in proportions of 50% and 50%. The extinction coefficient for C2H5Br at 147 nm and at 298 K has been determined as ∊ = (1/PL) In(Io/It) = 712 ± 7 atm-1 · cm-1.
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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. 707-724 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of labeled N15NO+ with CO, NO, O2, 18O2, N2, NO2, and N2O have been investigated using a tandem ICR instrument. In each case the total rate coefficient, product distribution, and kinetic energy dependence were measured. The results indicate that very specific reaction mechanisms govern these reactions. This conclusion is suggested by the lack of isotopic scrambling in many cases and by the complete absence of energetically allowed products in almost all of the systems. The kinetic energy studies indicate that most of the reaction channels proceed through an intermediate complex at low energies and via a direct mechanism at higher kinetic energies. Such direct mechanisms include long range charge transfer and atom or ion transfer.
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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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  • 81
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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. 835-847 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chlorocyclopropane has been produced by addition of CH2(1A1) and CH2(3B1) to chloroethene. CH2 was generated by the photolysis of ketene at 313 and 366 nm. Chlorocyclopropane was formed in a chemically activated state, had an energy content between 378 and 427 kJ/mol, and reacted in three parallel channels to 3-chloropropene, cis- and trans-1-chloropropene. As secondary reactions elimination of HCl from the chemically activated primary products occurred to form allene and propyne. The apparent rate constants for the isomerization and elimination reactions are reported. The results of RRKM calculations including distribution functions for the activated chlorocyclopropane and a stepladder model for the deactivation support the proposed reaction scheme.
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  • 83
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    International Journal of Chemical Kinetics 16 (1984), S. 801-816 
    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 thermal decomposition of n-propylsilane have been studied by the single pulse shock tube-comparative rate technique at pressures around 4700 torr between 1095-1240 K. The primary dissociation processes are 1,1 and 1,2 H2 elimination with ø1,1 ⋍ 0.75 and ø1,2 ⋍ 0.25, respectively. Subsequent decompositions of the primary process product, n-propylsilylene, to propylene and ethylene is complete even in the presence of excess butadiene. Possible mechanistic paths for these decompositions are discussed and an activation energy range of 30 ± 4 kcal is established for both processes. Induced decomposition via silylene chains accounts for 36-46% of the overall reaction in the uninhibited decomposition of n-propylsilane. The silylene chains are quenched in excess butadiene, and studies under maximum inhibition give overall decomposition kinetics of, log k(nPrSiD3, s-1) = 15.26-65,300 ± 1950 cal/2.303. Computer modeling results of the overall reaction both in the absence and presence of butadiene are also presented and shown to be in acceptable agreement with the experimental observations.
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  • 84
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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. 849-866 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An efficient process for converting the energy stored in electronically excited NF(a1Δ) into blue-green BiF (A—X) band emissions has been discovered. Bismuth atoms are converted to BiF and then repeatedly pumped to the (AO+) state in two steps via collisions with NF(a1Δ). A model has been formulated that predicts BiF emission intensities that are in excellent agreement with the observed values. Some of the rate coefficients required for this model are estimated by means of charge-transfer theories. The cyclic nature of this system, along with its other basic properties, suggests that it has a strong potential to be an efficient blue-green laser system.
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    International Journal of Chemical Kinetics 16 (1984), S. 867-878 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of OH reactions with furan (k1), thiophene (k2), and tetrahydrothiophene (k3), have been investigated over the temperature range 254-425 K. OH radicals were produced by flash photolysis of water vapor at λ 〉 165 nm and detected by timeresolved resonance fluorescence spectroscopy. The following Arrhenius expressions adequately describe the measured rate constants as a function of temperature (units are cm3 molecule-1 S-1): k1 = (1.33 ± 0.29) × 10-11 exp[(333 ± 67)/T], k2 = (3.20 ± 0.70) × 10-12 exp[(325 ± 71)/T], k3 = (1.13 ± 0.35) × 10-11 exp[(166 ± 97)/T]. The results are compared with previous investigations and their implications regarding reaction mechanisms and atmospheric residence times are discussed.
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    International Journal of Chemical Kinetics 16 (1984), S. 879-886 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative rate constants for the reactions of hydroxyl radicals with a series of alkyl substituted olefins were measured by competitive reactions between pairs of olefins at 298 ± 2 K and 1 atmospheric pressure. Hydroxyl radicals were produced by the photolysis of H2O2 with 254-nm irradiation. The obtained rate constants were (× 10-11 cm3 molecule-1 s-1): 2.53 ± 0.06, propylene; 5.49 ± 0.17, cis-2-butene; 5.47 ± 0.1, isobutene; 6.46 ± 0.13, 2-methyl-1-butene; 6.37 ± 0.16, cis-2-pentene; 6.23 ± 0.1, 2-methyl-1-pentene; 8.76 ± 0.14, 2-methyl-2-pentene; 6.24 ± 0.08, trans-4-methyl-2-pentene; 10.3 ± 0.1, 2,3-dimethyl-2-butene; 9.94 ± 0.1, 2,3-dimethyl-2-pentene; 5.59 ± 0.07, trans-4,4-dimethyl-2-pentene. A trend in alkyl substituent effect on the rate constant was found, which is useful to predict kOH on the basis of the number of alkyl substituents on the double bond.
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    International Journal of Chemical Kinetics 16 (1984), S. 899-907 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of ground-state S(3PJ) atoms with thiirane, methylthiirane, and trans-2,3-dimethylthiirane have been studied by flash photolysis-VUV kinetic absorption spectroscopy. From the analysis of the S(3PJ) decay plots the following rate constants were determined: (1.4 ± 0.2) × 1013, (2.7 ± 0.3) × 1013 and (4.0 ± 0.2) × 1013 (in cm3 mol-1 s-1 units) for thiirane, methylthiirane and trans-2,3-dimethylthiirane, respectively, showing an upward trend with increasing methylation.
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    International Journal of Chemical Kinetics 16 (1984), S. 887-898 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants have been determined at 296 ± 2 K for the gas phase reaction of NO3 radicals with a series of aromatics using a relative rate technique. The rate constants obtained (in cm3 molecule-1 s-1 units) were: benzene, 〈2.3 × 10-17; toluene, (1.8 ± 1.0) × 10-17; o—xylene, (1.1 ± 0.5) × 10-16; m—xylene, (7.1 ± 3.4) × 10-17; p—xylene, (1.4 ± 0.6) × 10-16; 1,2,3-trimethylbenzene, (5,6 ± 2.6) × 10-16; 1,2,4-trimethylbenzene (5.4 - 2.5) × 10-16; 1,3,5-trimethylbenzene, (2.4 ± 1.1) × 10-16; phenol, (2.1 ± 0.5) × 10-12; methoxybenzene, (5.0 ± 2.8) × 10-17; o-cresol, (1.20 ± 0.34) × 10-11; m-cresol, (9.2 ± 2.4) × 10-12; p-cresol, (1.27 ± 0.36) × 10-11; and benzaldehyde, (1.13 ± 0.25) × 10-15. These kinetic data, together with, in the case of phenol, product data, suggest that these reactions proceed via H-atom abstraction from the substituent groups. The magnitude of the rate constants for the hydroxy-substituted aromatics indicates that the nighttime reaction of NO3 radicals with these aromatics can be an important loss process for both NO3 radicals and these organics, as well as being a possible source of nitric acid, a key component of acid deposition.
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    International Journal of Chemical Kinetics 16 (1984), S. 909-918 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constants for reversible addition of the substituted phenylthio radicals to vinylpyridines in solution at 23°C have been determined by flash photolysis method. For each phenylthio radical, the reactivities of vinylpyridines is 3-5 times lower than that of styrene. The relative equilibrium constants estimated with flash photolysis indicate that the stabilities of the adduct carbon-centered radicals generated from vinylpyridines are similar to that from styrene. The Hammett plots suggest that the difference in the reactivities originates in the polar transition state; the nitrogen atom in 4-vinylpyridine withdraws the electrons of vinylic double bond.
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    International Journal of Chemical Kinetics 16 (1984), S. 941-945 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NO Abstract.
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    Keywords: Chemistry ; Physical Chemistry
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    International Journal of Chemical Kinetics 16 (1984), S. 919-939 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation of nitrous acid (HONO) in the dark from initial concentrations of NO2 of 0.1-20 ppm in air, and the concurrent disappearance of NO2, were monitored quantitatively by UV differential optical absorption spectroscopy in two different environmental chambers of ca.4300- and 5800-L volume (both with surface/volume ratios of 3.4 m-1). In these environmental chambers the initial HONO formation rate was first order in the NO2 concentration and increased with the water vapor concentration. However, the HONO formation rate was independent of the NO concentration and relatively insensitive to temperature. The initial pseudo-first-order consumption rate of NO2 was (2.8 ± 1.2) × 10-4 min-1 in the 5800-L Teflon-coated evacuable chamber and (1.6 ± 0.5) × 10-4 min-1 in a 4300-L all-Teflon reaction chamber at ca.300 K and ca.50% RH. The initial HONO yields were ca.40-50% of the NO2 reacted in the evacuable chamber and ca.10-30% in the all-Teflon chamber. Nitric oxide formation was observed during the later stages of the reaction in the evacuable chamber, but ca.50% of the nitrogen could not be accounted for, and gas phase HNO3 was not detected. The implications of these data concerning radical sources in environmental chamber irradiations of NOx- organic-air mixtures, and of HONO formation in polluted atmospheres, are discussed.
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    International Journal of Chemical Kinetics 16 (1984), S. 1103-1110 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results obtained from the photolysis of ketene with acetylene strongly support the formation of C3H3 radicals in the title reaction. Stationary state studies are interpreted in terms of the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm C}_3 {\rm H}_{\rm 4}^{\rm *} \buildrel3\over\rightarrow{\rm C}_3 {\rm H}_3^ \cdot + {\rm H}^ \cdot$$\end{document} with a rate constant (109.8 s-1) which is compared to RRKM predictions. In pulsed laser induced decomposition experiments, recombination products involving C3H3 have been detected (some for the first time) and their formation modeled using step (3) with the same rate constant.
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    International Journal of Chemical Kinetics 16 (1984), S. 1111-1115 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the self- and cross-termination of the isopropylol radical [(CH3)2ĊOH] and its anion [(CH3)2ĊO-] in aqueous solution are determined by kinetic electron spin resonance. Whereas the self-termination of the neutral radical occurs close to the diffusion-controlled limit, the cross- and self-terminations involving the anion are slower and reflect effects of charge repulsion and steric constraints by solvation.
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    International Journal of Chemical Kinetics 16 (1984), S. 1151-1160 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constant for the OH + HCl reaction has been measured from 240 to 295 K utilizing the techniques of laser/flash photolysis-resonance fluorescence. The HCl concentrations were monitored continuously by ultraviloet and infrared spectrophotometry. The results can be fit to the following Arrhenius expression: \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (4.6{\rm } \pm {\rm }0.3){\rm } \times {\rm }10^{ - 12} \exp [- (500{\rm } \pm {\rm }60)/T{\rm cm}^3 /{\rm molecule} \cdot {\rm s}$$\end{document} The rate constant values obtained in this study are 20-30% larger than those recommended previously for modeling of stratospheric chemistry.
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    International Journal of Chemical Kinetics 16 (1984), S. 1139-1150 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unimolecular decomposition of methyl nitrite in the temperature range 680-955 K and pressure range 0.64 to 2.0 atm has been studied in shock-tube experiments employing real-time absorption of CW CO laser radiation by the NO product. Computer kinetic modeling using a set of 23 reactions shows that NO product is relatively unreactive. Its initial rate of production can be used to yield directly the unimolecular rate constant, which in the fall-off region, can be represented by the second-order rate coefficient in the Arrhenius form: \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = 10^{17.90 \pm 0.21} \exp (- 17200 \pm 400/T){\rm cm}^{\rm 3} {\rm mol}^{ - 1} {\rm s}^{ - 1}$$\end{document} A RRKM model calculation, assuming a loose CH3ONO≠ complex with two degrees of free internal rotation, gives good agreement with the experimental rate constants.
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    International Journal of Chemical Kinetics 16 (1984), S. 1161-1166 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction \documentclass{article}\pagestyle{empty}\begin{document}${\rm Br} + {\rm CH}_3 {\rm CHO}\buildrel1\over\rightarrow{\rm HBr} + {\rm CH}_3 {\rm CO}$\end{document} has been studied by VLPR at 300 K. We find k1 = 2.1 × 1012 cm3/mol s in excellent agreement with independent measurements from photolysis studies. Combining this value with known thermodynamic data gives k-1 = 1 × 1010 cm3/mol s. Observations of mass 42 expected from ketene suggest a rapid secondary reaction: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm Br} + {\rm CH}_3 {\rm CO}\buildrel2\over\rightarrow[{\rm CH}_3 {\rm COBr}]^* \buildrel3\over\rightarrow{\rm HBr} + {\rm CH}_2 {\rm CO}$$\end{document} in which step 2 is shown to be rate limiting under VLPR conditions and k2 is estimated at 1012.6 cm3/mol s from recent theoretical models for radical recombination. It is also shown that 0 ≤ E1 ≤ 1.4 kcal/mol using theoretical models for calculation of A1 and is probably closer to the lower limit. Reaction -1 is negligible under conditions used.
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    International Journal of Chemical Kinetics 16 (1984), S. 1167-1173 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Potassium persulfate oxidizes triphenylphosphine to triphenylphosphine oxide in 60% aqueous acetonitrile. It has been suggested that the oxygen of the product, triphenylphosphine oxide, might originate from solvent water, following nucleophilic attack on an intermediate phosphonium ion. We have investigated the origin of the oxygen in the oxidation of triphenylphosphine by potassium persulfate in 60% aqueous acetonitrile containing 20% [18O]water. The product was analyzed by using the 18O isotope effect in 31P NMR spectroscopy. The magnitude of the 18O isotope-induced shift was determined by synthesizing triphenylphosphine [18O]oxide and was found to be 0.038 ppm upfield. The product of the oxidation reaction in 20% [18O]water displayed no 18O isotope effect. The origin of the oxygen in the oxidation reaction is the persulfate ion, consistent with an alternative mechanism involving nucleophilic attack by water at the sulfur atom of a phosphonium peroxysulfate intermediate.
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