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  • 1985-1989  (346)
  • 1988  (137)
  • 1987  (91)
  • 1985  (118)
  • Physical Chemistry  (346)
  • 101
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 177-186 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of esters using the flash photolysis resonance fluorescence technique. Experiments were performed over the temperature range 240-440 K at total pressures (using Ar diluent gas) between 25-50 torr. The kinetic data for methyltrifluoroacetate (k1) over the complete temperature range, and for methylacetate (k2), and ethylacetate (k3) over the range 296-440 K were used to derive the Arrhenius expressions; \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (3.0 \pm 0.7) \times 10^{- 13} {\rm \,exp[- (512} \pm {\rm 78)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_2 = (8.3 \pm 3.5) \times 10^{- 13} {\rm \,exp[- (260} \pm 150{\rm)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_3 = (2.3 \pm 0.2) \times 10^{- 12} {\rm \,exp[- (131} \pm 28{\rm)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} At 296 K, the measured rate constants (in units of 10-13 cm3 molecule-1 s-1) were: k1 = (0.52 ± 0.08), k2 = (3.41 ± 0.29), and k3 = (15.1 ± 1.4). Room temperature rate constants for the OH reactions with several other aliphatic esters were also measured. These were (in the above units): methylformate, (2.27 ± 0.34); ethylformate, (10.2 ± 1.4); n-propylformate, (23.8 ± 2.7); n-butylformate, (31.2 ± 3.3); n-propylacetate, (34.5 ± 3.4); i-propylacetate, (37.2 ± 2.9); n-butylacetate, (41.5 ± 3.0); s-butylacetate, (56.5 ± 5.9); methylpropionate, (10.3 ± 0.4); ethylpropionate, (21.4 ± 3.0); n-propylpropionate, (40.2 ± 3.2); methylbutyrate, (30.4 ± 3.3); ethylbutyrate, (49.4 ± 3.8); n-propylbutyrate, (74.1 ± 3.2), and n-butylbutyrate, (106 ± 13), error limits represent 2σ from linear least-squares analyses. The results are discussed in terms of the reaction mechanisms and are compared to previous literature data.
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  • 102
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 273-281 
    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 reactions of the OH radical with (C2H5O)3PO and (CH3O)2P(S)Cl and of the reactions of NO3 radicals and O3 with (CH3O)2P(S)Cl have been studied at room temperature. Using a relative rate technique, the rate constants determined for the reactions of the OH radical with (C2H5O)3PO and (CH3O)2P(S)Cl at 296 ± 2 K and 740 torr total pressure of air were (5.53 ± 0.35) × 10-11 and (5.96 ± 0.38) × 10-11 cm3 molecule-1 s-1, respectively. Upper limits to the rate constants for the NO3 radical and O3 reactions with (CH3O)2P(S)Cl of 〈3 × 10-14 cm3 molecule-1 s-1 and 〈2 × 10-19 cm3 molecule-1 s-1, respectively, were obtained. These data are compared and discussed with previous literature data for organophosphorus compounds.
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  • 103
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 455-466 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new estimate is derived for the group additivity contribution ΔHƒ∘[O - (O)2] = 55 ± 6 kJ mol-1, based upon recent experimental data, which enables heats of formation and bond dissociation energies to be estimated for species ROnR and ROn¨(R = H, CH3, and CF3). Semi-empirical MNDO calculated heats of formation, for these species, provide independent support for the new thermochemical estimates. The results are also consistent with other theoretical and experimental evidence.
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  • 104
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 131-144 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constant for the Br + O3 → BrO + O2 reaction was measured by the discharge flow technique, employing resonance fluorescence detection of Br. Over the temperature range 248 to 418 K, in 1 to 3 torr of He, decays of Br in excess O3 yield the value k1 = (3.28 ± 0.40) × 10-11 e[-944±30]/T cm3 molecule-1 s-1. Cited uncertainties are at the 95% confidence level and include an estimate of the systematic errors. The rate constants for the reactions of O3 with Br, Cl, F, OH, O, and N correlate with the electron affinities of the radicals suggesting that the reactions proceed through early transition states dominated by transfer of electron density from the highest occupied molecular orbital of ozone to the singly occupied radical MO. The implications of this new measurement of k1 for stratospheric chemistry are discussed.
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  • 105
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 106
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 195-215 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general numerical method and program for simulation of the kinetics of multistep reactions is described, with details for collation of data, construction of a mechanistic model, and simulation of reciprocal relaxation times and calculation of individual rate constants. The working scheme of the program includes an initial approximate simulation by adjustment of the rate constants followed by their optimization with a Powell minimization subroutine. The procedure is applied to aromatic nucleophilic addition.
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  • 107
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 241-265 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and products of the homogeneous gas-phase reactions of the OH radical with the chloroethenes were investigated at 298 ± 2 K and atmospheric pressure. Using a relative rate technique and ethane as a scavenger for the chlorine atoms produced in these OH radical reactions, rate constants (in units of 10-12 cm3 molecule-1s-1) of 8.11 ± 0.24, 2.38 ± 0.14, and 1.80 ± 0.03 were obtained for 1,1-dichloroethene, cis-1, 2-dichloroethene and trans-1,2-dichloroethene, respectively. Under these conditions, the major products observed by long pathlength FT-IR absorption spectroscopy were HCHO and HC(O)Cl from vinyl chloride; HC(O)Cl from cis- and trans-1,2-dichloroethene; HCHO and COCl2 from 1,1-dichloroethene; HC(O)Cl and COCl2 from trichloroethene; and COCl2 from tetrachloroethene. In the absence of a Cl atom scavenger, significant yields of the chloroacetyl chlorides, CHxCl3-xC(O)Cl, were observed from 1,1-dichloro-, trichloro- and tetrachloroethene, indicating that these products resulted from reactions involving chlorine atoms. The yields of all of these products are reported and the mechanisms of these gas-phase reactions discussed. In addition, OH radical reaction rate constants were redetermined, in the presence of a Cl atom scavenger, for cis- and trans-1,3-dichloropropene and 3-chloro-2-chloromethyl-1-propene, being (in units of 10-12 cm3 molecule-1 s-1) 8.45 ± 0.41, 14.4 ± 0.8, and 33.5 ± 3.0, respectively.
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  • 108
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 339-342 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 109
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 365-378 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hexacyanoferrate(III)-thallium(I) reaction in aqueous acetic acid containing large concentrations of hydrochloric acid is considerably accelerated both by hydrogen and chloride ions as well as increasing acetic acid in the medium. The experimental results obey the rate law (1) where β1 to β6 \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{rcl} {{\rm (1)}} & {- \frac{{{\rm d[Fe(CN)}_{\rm 6} ^{{\rm 3 -}}]}}{{dt}} = \frac{{\{\beta _4 k_a [{\rm H}^ +] + \beta _5 k_b [{\rm H}^ +]^2 \} \beta _2 [{\rm Cl}^ -]^2 [{\rm Fe(CN)}_{\rm 6} ^{{\rm 3 -}}]_T [Tl^ +]_T}}{{\{1 + \beta _4 [{\rm H}^ +] + \beta _5 [{\rm H}^ +]^2 + \beta _6 [{\rm H}^ +]^3 \} \{1 + \beta _1 [{\rm Cl}^ -] + \beta _2 [{\rm Cl}^ -]^2 + \beta _2 [{\rm Cl}^ -]^3 \}}}}\end{array}$$\end{document} are the cumulative stability constants of the species TlCl, TlCl2-, TlCl32-, HFe(CN)62-, H2Fe(CN)6- and H3Fe(CN)6 respectively and ka and kb are the rate constants associated with the mono- and di-protonated oxidant species. The main active species are H2Fe(CN)6- and TlCl2-.
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  • 110
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 397-409 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chlorinations of dimethylamine, diethylamine, methylethanolamine, ethylethanolamine and diethanolamine by N-chlorosuccinimide have been found to be equilibrium reactions of order one with respect to both N-chlorosuccinimide and amine in the forward direction and of order one with respect to succinimide and the resulting N-chloramine in the other. These results are explained by postulating a mechanism in which the rate controlling step consists in direct exchange of positive chlorine between the N-chlorosuccinimide and the amine.
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  • 111
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Elementary bimolecular processes that involve formation of a chemically activated intermediate species are common. We address the general problem of modeling these processes and describe the necessary and sufficient information that must be specified to assure that a kinetics model will extrapolate the rate constants for those reactions over wide ranges of temperature and pressure. The approach is illustrated for the system centered around the HOCO intermediate. Here, specification of the temperature and pressure dependence of three rate constants, k(T,P) and the temperature dependence of two equilibrium constants, K(T), is necessary and sufficient, viz: Rate constants are cast in the form of an analytical expression, suggested by Troe, and appropriate parameters are tabulated.
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  • 112
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 113
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 103-110 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The temperature dependence of the rate of the reaction of OH with 2-(dimethylamino)-ethanol, (CH3)2NCH2CH2OH (DMAE) was investigated over the temperature range, 234 to 364 K. The reaction was studied using the flash photolysis-resonance fluorescence technique. The room temperature rate constant determined for this reaction was (10.3 ± 2.0) × 10-11 cm3 molecule-1 s-1, with essentially no temperature dependence evident within the uncertainty in the experiments. A value of (9.0 ± 2.0) × 10-11 cm3 molecule-1 s-1 is believed to best describe the reaction over the entire temperature range. The room temperature rate constant is about twice the value reported previously for this reaction. The overall reaction of OH with DMAE was apportioned to the reactivity of OH for abstracting individual H- atoms from different types of C—H bonds and the O—H bond within the molecule. This technique predicts the overall rate constant for the OH-DMAE reaction to within about 15% of the experimental value and makes it possible to estimate the yields of the initial radical products of the OH attack on DMAE. A mechanism is proposed for the subsequent atmospheric reactions that would occur in the photooxidation of DMAE.
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  • 114
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 145-151 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of elimination of seven cycloalkyl acetates containing between 5 and 15 ring carbons have been determined in a static system over a temperature range 280-370°C and a pressure range 35-234 torr. The unimolecular reactions, carried out in the presence of the inhibitor cyclohexene, are homogeneous in seasoned vessels and follow a first-order rate law. The rate coefficients are exemplified by that found for cyclopentyl acetate: \documentclass{article}\pagestyle{empty}\begin{document}$$\log {\rm}k_1 ({\rm s}^{{\rm - 1}}) = (12.68 \pm 0.14) - (179.8 \pm 1.5){\rm \,kJ\,mol}^{{\rm - 1}} {\rm (2}{\rm .303}RT)^{- 1}$$\end{document} The sequence of relative rates is analogous to that found in most solution reactions of these compounds. The contribution of ring strain to energy barriers of these compounds is described.
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  • 115
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    International Journal of Chemical Kinetics 20 (1988), S. 217-222 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flash vacuum pyrolysis of (β-chloro ethyl)-pyrazole was studied. Pyrazole elimination and vinyl chloride formation were found. Competitive reactions with (β-chloro ethyl)-pyrazole were carried out using N-ethyl-3,5-dimethyl pyrazole as internal standard to obtain the kinetic parameters (Ea). Δ(ΔHƒ∘) for this reaction was calculated.
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  • 116
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    International Journal of Chemical Kinetics 20 (1988), S. 501-511 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of oxidation of ethylene glycol and glycerol by acidic solution of N-bromoacetamide (NBA) in the presence of ruthenium (III) chloride as a homogeneous catalyst and mercuric acetate as scavenger in the temperature range of 30-50°C have been reported. The reactions follow identical kinetics, being zero-order in substrate and first-order in Ru(III). First order dependence of the reaction on NBA at its low concentrations tends to zero order in the higher concentration range. Positive effect of [H-] and [Cl-] has been observed. A negative effect of acetamide and ionic strength of the medium is observed while D2O and mercuric acetate show zero effect on the reaction velocity. Various activation parameters have been computed. The main product of the oxidation is corresponding acid. (H2OBr)+ has been postulated as the oxidizing species. A suitable mechanism in conformity with the kinetic data has been proposed.
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  • 117
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    International Journal of Chemical Kinetics 20 (1988), S. 565-575 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase kinetics of the bromine catalyzed elimination of HCl from 1,1,1-trichloroethane has been studied over a five fold variation of (CH3CCl3)/(Br2) and from 565 to 634 K. The most important reactions in the mechanism are found to be: The preferred analysis of the kinetic data results in log(k1/M-1 s-1) = 11.3 ± 0.3 - (19.9 ± 1.0) × 103/4.575 T. From these results one calculates the C - H bond dissociation energy in CH3CCl3 to be 103.8 ± 2 kcal mol-1, and the heat of formation of 2,2,2-trichloroethyl to be 17.7 ± 2 kcal mol-1.
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  • 118
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the recombination reaction OD + NO2 + M → DNO3 + M have been determined in the falloff region (5-500 torr) and at 297 ± 2 K, in the presence of He, N2, and SF6 as third bodies, by using a pulsed laser photolysis-resonance absorption technique. Values of k0, kx and the falloff parameter Fc have been estimated. Our rate constants were, within the experimental uncertainty, the same as those reported for the reaction of OH radicals with NO2.
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  • 119
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 120
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 699-712 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the interactions of the Keggin type heteropolyanion [CoW12O40]5-, with all the molecular and anionic forms of citric acid have been investigated spectrophotometrically in the pH range 0.60-5.45 at 60°C. With the exception of the molecular form of the acid (H3L), all the other species (H2L-, HL2-, and L3-) undergo oxidation through an alkali metal ion catalyzed path in addition to the uncatalyzed one. The catalytic power increases with increasing size of the alkali metal ion. The contributions of each path have been evaluated from the kinetic data with the help of the measured dissociation constant values of citric acid. A plausible mechanism involving the formation of a bridged outer-sphere complex of the reacting species with the alkali cation, has been suggested. The observed limiting dependence of kobs on [citrate] at high concentrations owing to an equilibrium between the reactants preceeding the electron transfer step supports the proposed mechanism. The pH-rate profile gives an excellent fit with the evaluated kinetic parameters.
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  • 121
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    International Journal of Chemical Kinetics 20 (1988), S. 827-827 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 122
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 123
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    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 849-855 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Taylor dispersion technique has been used to measure the diffusion coefficients of nine compounds in dilute solution in isopropanol at 300 K. These compounds correspond, by the difference of a single hydrogen atom, to nine free radicals, for which the rate constants for bimolecular (termination) reactions have been previously measured under the same conditions by e.s.r. Comparison of the two sets of results show the termination reactions to be essentially diffusion-controlled, and, assuming no activation-energy effect, interaction parameters for the termination reactions are calculated and discussed.
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  • 124
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    International Journal of Chemical Kinetics 20 (1988), S. 815-826 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ultraviolet absorption spectra of chloromethylperoxy and fluoromethylperoxy radicals, CH2ClO2 and CH2FO2, and the kinetics of their respective self reactions have been studied in the gas phase using a flash photolysis technique. The absorption spectra for both radicals were quantified over the wavelength range 210 and 290 nm. The measured absorption cross-sections \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} \sigma _{{\rm CH}_{\rm 2} {\rm ClO}_{\rm 2}} (250{\rm nm)} = (3.14 \pm 0.45) \times 10^{- 18} {\rm cm}^{\rm 2} {\rm molecule}^{- 1} \\ \sigma _{{\rm CH}_{\rm 2} {\rm FO}_{\rm 2}} (240{\rm nm)} = (3.72 \pm 0.45) \times 10^{- 18} {\rm cm}^{\rm 2} {\rm molecule}^{- 1} \\ \end{array} $$\end{document} were used to derive the observed self-reaction rate constants (for reactions 1 and 2) over the temperature range 228-380 K, defined as -d[CH2XO2]/dt = 2k[CH2XO2]2, where X represents Cl or F. The rate constants at 298 K were found to be independent of pressure over the range 25-400 torr N2 with values of k1(298 K) = (3.78 ± 0.45) × 10-12 and k2(298 K) = (3.07 ± 0.65) × 10-12 in units of cm3 molecule-1 s-1. The kinetic data over the complete temperature range are represented by the Arrhenius expressions: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k_1 = (3.1 \pm 1.1) \times 10^{- 13} \exp [(735 \pm 95)/{\rm T] cm}^{\rm 3} {\rm molecule}^{- 1} {\rm s}^{- 1} \\ k_2 = (3.3 \pm 1.2) \times 10^{- 13} \exp [(700 \pm 100)/{\rm T] cm}^{\rm 3} {\rm molecule}^{- 1} {\rm s}^{- 1} \\\end{array} $$\end{document} where the error limits represent 2σ from linear least squares analysis. These results are discussed with respect to previous measurements of the absorption spectra and reactions of alkylperoxy radicals.
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  • 125
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Modified Simplex Method (MSM) coupled with contour diagrams is used to determine the rate constants of a kinetic scheme involving three sequential second order processes.Reaction between glutathione and the dithiocarbamate fungicide tetramethylthiuram disulfide produces the oxidized form of glutathione which is then reduced in the presence of NADPH. The concentration of the reducing agent is monitored as a function of time. In the absence of simplifying assumption a closed form solution of the rate equations does not exist. Computed curves of NADPH concentration versus time were generated using the software SIMULCIN.The rate constant values are optimized by the MSM procedure to obtain the best agreement between calculated and experimental data. The significance, validity limits of the estimated rate constants and the relevance of these in vitro data to previous in vivo studies are discussed.
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  • 126
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    International Journal of Chemical Kinetics 20 (1988), S. 857-866 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of reaction between NO and HNO3 and the rate of thermal decomposition of HNO3 have been measured by FTIR spectroscopy. The measurements were made in a teflon lined batch reactor having a surface to volume ratio of 14 m-1. During the experiments, with initial HNO3 concentrations between 2 and 12 ppm and NO concentrations between 2 and 30 ppm, a reactant stoichiometry of unity and a first order NO and HNO3 dependence were confirmed. The observed rate constant for the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm HNO}_{\rm 3} + {\rm NO} \longrightarrow {\rm HNO}_{\rm 2} + {\rm NO}_2$$\end{document} at 22°C and atmospheric pressure was determined to 1.1 (±0.3) 10-5 ppm-1 min-1. At atmospheric pressure, HNO3 decomposes into NO2 and other products with a first order HNO3 dependence and with a rate constant of 2.0 (±0.2) 10-3 min-1. The apparent activation energy for the decomposition is 13 (±4) kJ mol-1.
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  • 127
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    International Journal of Chemical Kinetics 20 (1988), S. 885-895 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 147 nm photolysis of 3,3 dimethylbut-1-ene leads mainly to the formation of very hot (≅375 kJ/mol) α,α-dimethallyl radicals. On the other hand, that of 3-methyl-cis-and trans-pentene-2, as well as that of 2,3-dimethylbut-1-ene is a source of very hot α,β-dimethallyl radicals. These allylic radicals are coolled down using pressure and are allowed to combine with available methyl radicals. From the formation of various C6H12 products, it is concluded that the very hot α,α- radical isomerizes towards the α,β-structure at low pressures and vice versa. The equilibrium constant of the following process has been evaluated to be 1.72 ± 0.30. \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CH}_3{\rm C}({\rm CH}_3){\rm CHCH}_2 ^ * \Leftrightarrow {\rm CH}_2 {\rm C}({\rm CH}_{\rm 3}){\rm CHCH}_3 ^ *$$\end{document}
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  • 128
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    International Journal of Chemical Kinetics 20 (1988), S. 877-884 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of poly(4-vinylbiphenyl) (denoted as PVB) polymers and biphenyl molecules with solvated electrons in the 2-methyltetrahydrofuran (MTHF) solvent have been studied at 100-120 K by electron-pulse radiolysis. The formation of PVB polymer anions as well as biphenyl anions was observed by the electron-pulse irradiation of the MTHF-PVB(or biphenyl) solution. The anions are formed by two processes; a rapid formation during the pulse irradiation (〈20 ns) and a slow formation after the pulse irradiation. The slow formation is due to a diffusion-controlled reaction between solutes, such as PVB and biphenyl, and solvated electrons. It was found that the reaction efficiency, expressed in monomer unit, of PVB polymers is 1/27 of that of biphenyl molecules. The reaction radius for the electron capture reaction of PVB polymers is estimated as 200-370 A, which is much larger than the gyration radius (107 A) of polymer coils in MTHF solution.
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  • 129
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    International Journal of Chemical Kinetics 20 (1988), S. 867-875 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative rate technique has been used to determine the rate constants for the reaction of chlorine atoms with a series of oxygenated organic species. Experiments were performed at 295 ± 2 K and atmospheric pressure of synthetic air or nitrogen. The decay rates of the organic species were measured relative to that of ethane or n-butane. Using rate constants of 5.7 × 10-11 cm3 molecule-1 s-1, and 2.25 × 10-10 cm3 molecule-1 s-1 for the reaction of Cl with ethane and n-butane respectively the following rate constants were derived, in units of 10-11 cm3 molecule-1 s-1: propane, (16.0 ± 0.4);i-butane, (15.1 ± 0.9) n-pentane, (31.0 ± 1.6); n-hexane, (34.5 ± 2.3); cyclohexane, (36.1 ± 1.5); methanol, (4.57 ± 0.40); ethanol, (8.45 ± 0.91); n-propanol, (14.4 ± 1.2); t-butylalcohol, (3.26 ± 0.19); acetaldehyde, (8.45 ± 0.79); propionaldehyde, (11.3 ± 0.9); dimethylether, (20.5 ± 0.8); diethylether, (35.6 ± 2.8); and methyl-t-butylether, (16.6 ± 1.2). Quoted errors represent 2σ, and do not include any errors due to uncertainties in the rate constants used to place our relative measurements on an absolute basis. The results are discussed with respect to the mechanisms of these reactions and to previous literature data.
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  • 130
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    International Journal of Chemical Kinetics 20 (1988), S. 897-907 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic study of the reactions of H atoms with CH3SH and C2H5SH has been carried out at 298 K by the discharge flow technique with EPR and mass spectrometric analysis of the species. The pressure was 1 torr. It was found: k1 = (2.20 ± 0.20) × 10-12 for the reaction H + CH3SH (1) and k2 = (2.40 ± 0.16) × 10-12 for the reaction H + C2H5SH (2). Units are cm3 molecule-1 s-1. A mass spectrometric analysis of the reaction products and a computer simulation of the reacting systems have shown that reaction (1) proceeds through two mechanisms leading to the formation of CH3S + H2 (1a) and CH3 + H2S (1b).
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  • 131
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    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 132
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    International Journal of Chemical Kinetics 20 (1988), S. 915-938 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The generation of metastable O2(1Σg+) and O2(1Δg) in the H + O2 system of reactions was studied by the flow discharge chemiluminescence detection method. In addition to the O2(1Σg+) and O2(1Δg) emissions, strong OH(v = 2) → OH(v = 0), OH(v = 3) → OH(v = 1), HO2(2A′000) → HO2(2A″000), HO2(2A′001) → HO2(2A″000), and H O2(2A″200) → HO2(2A″000) emissions were detected in the H + O2 system. The rate constants for the quenching of O2(1Σg+) by H and H2 were determined to be (5.1 ± 1.4) × 10-13 and (7.1 ± 0.1) × 10-13 cm3 s-1, respectively. An upper limit for the branching ratio to produce O2(1Σg+) by the H + HO2 reaction was calculated to be 2.1%. The contributions from other reactions producing singlet oxygen were investigated.
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  • 133
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    International Journal of Chemical Kinetics 20 (1988), S. 939-955 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A flow system has been developed to study relative rate coefficients of hydroxyl radicals reacting with alkanes under conditions relating to tropospheric chemistry. Relative Arrhenius parameters have been measured over the temperature range 243-328 K for pairs of alkanes from a list consisting of n-butane, 2-methylpropane, n-pentane, n-hexane, 2,2- and 2,3-dimethylbutane, 2,3,3-trimethylbutane, and 2,3,4-trimethylpentane.The results have been incorporated into a Structure-Activity Relation for hydroxylalkane reactions which leads to the following group rate coefficients for a temperature range of 240-500 K. \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{rcl} k_{{\rm prime}}^0 &=& 3.13 \times 10^{ - 12}\, {\rm exp(} - 904/T)\,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \\ k_{{\rm sec}}^0 &=& 2.45 \times 10^{ - 12} \,{\rm exp(} - 320/T)\,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \\ k_{{\rm tert}}^0 &=& 1.88 \times 10^{ - 12} \,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \end{array}$$\end{document}
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  • 134
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    International Journal of Chemical Kinetics 20 (1988), S. 26-26 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 135
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    International Journal of Chemical Kinetics 20 (1988), S. 967-978 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterogeneous recombination of O + CO → CO2 over a solid CO2 surface at 77 K was investigated. A modified discharge flow setup was used to generate low O atom concentrations by the reaction N + NO → N2 + O(3P). The O atom concentrations were measured upstream and downstream of the solid CO2 substrate using resonance fluorescence by monitoring the unresolved 130.3 nm triplet transition 3S1 - 3P2,1,0 at the two fixed points. CO2 formed was determined by measuring the β activity from C14O2 produced from CO containing C14O as a reactant gas. The CO2 formation was found to be first order in CO and independent of O atom concentration over the entire range of 4.3 × 1012 to 1.9 × 1014 cm-3 and 1.2 × 1011 to 5.6 × 1012 cm-3 for CO and O respectively. The first order recombination coefficient, λCO was found to be 1.4 (±.38) × 10-5.
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  • 136
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    International Journal of Chemical Kinetics 20 (1988), S. 379-386 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal isomerization of azulene was studied in shock waves over the range 1300-1900 K. Monitoring azulene and naphthalene light absorptions in the UV, a complete conversion azulene → naphthalene was observed. After correction for some falloff effects, a limiting high pressure rate constant kx = 1012.93 exp(-263 kJ mol-1/RT) s-1 was derived. Based on this kx, specific rate constants k(E) for photoexcitation experiments were constructed.
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  • 137
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    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 138
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    International Journal of Chemical Kinetics 19 (1987), S. 457-486 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A chemical kinetic reaction mechanism has been developed which describes the oxidation of propanal within the temperature range 400-700 K. This mechanism has been tested against data obtained by four experimental groups over a wide range of initial conditions. The induction period and the absolute rate of propanal consumption are predicted to within a factor of 2 for initial densities of oxygen and propanal ranging over factors of 400. The existence and location of the negative temperature coefficient in the consumption of propanal are also simulated properly. The yields of all major and most minor products are predicted to within a factor of 2 for the wide variety of initial conditions tested. Sensitivity analyses were carried out at 553 and 713 K to identify the reactions primarily responsible for controlling the rate of propanal consumption and the distribution of products.
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  • 139
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    International Journal of Chemical Kinetics 19 (1987), S. 503-512 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction IO + CH3SCH3 → products (3) was studied at room temperature and near 1 Torr pressure of He, using the discharge flow mass spectrometric technique. The rate constant was found to be k3 = (1.5 ± 0.5) × 10-11 cm3 molecule-1 s-1. CH3S(O)CH3 was detected as a product suggesting the following channel: IO + CH3SCH3 → CH3S(O)CH3 + I. The rate constant of the reaction IO + IO → products (1) was also measured: k1 = (3 ± 0.5) × 10-11 at 298 K and 1 Torr pressure. The atmospheric implication of reaction (3) is discussed. The results indicate that this reaction could be a potential important sink of CH3SCH3 in marine atmosphere.
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  • 140
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    International Journal of Chemical Kinetics 19 (1987), S. 571-578 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic study of the gas-phase thermal elimination reactions of N-ethyl-3,5 dimethyl-pyrazole (I), N-ethyl-pyrazole (II), N-sec-butyl-pyrazole (III), and N-tert-butyl-pyrazole (IV) using a flow system is reported. After obtaining activation parameters for I we carried out competitive reactions with II, III and IV using I as internal standard to obtain their Ea. The values of Δ(ΔHfo) calculated for II, III and IV agree with the little differences in Ea experimentally found.
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  • 141
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the reaction of oxiranes with bis/2-hydroxyalkyl/disulfides, bis/2-Hydroxyalkyl/sulfides, and 1,6-Hexanediol in the presence of N,N-dimethylcyclohexylamine were studied at the temperature range of 50-90°C. A mechanism of these reactions has been proposed and its kinetic equation has been presented.
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  • 142
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    International Journal of Chemical Kinetics 19 (1987), S. 639-647 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser-controlled bimolecular isotopic exchange reactions in bromine leading to alterations in natural isotopic abundance ratios have been directly observed using laser-modulated molecular beams and mass analysis. Several instances of selective excitation and subsequent rapid isotope exchange are observed within the 7 GHz gain curve of the exciting 514.5 nm line of an argon-ion laser. These exchange processes are attributed to the direct photochemical participation of excited molecular states in the B3Πou+ system of Br2.
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  • 143
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    International Journal of Chemical Kinetics 19 (1987), S. 659-678 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of acetylene-styrene mixtures has been studied from 450-550°C in a quartz reaction vessel in the absence and presence of O2 or NO. The rates of disappearance of reactants and formation of adducts are first-order in each reactant. The major product is polymer, with the adducts accounting for about 2.5% and 6.2% of the styrene removed at 450 and 550°C, respectively. The acetylene-to-styrene removal ratio is about 27 independent of temperature. The adducts formed are methyl indene and 1,2-dihydronaphthalene. These are about half-suppressed in the presence of O2 or NO. The rate coefficients for reactant removal and adduct formation are: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{\rm 2} {\rm H}_{\rm 2} \},M^{ - 1} {\rm s}^{ - 1} \} = 7.53 \pm 0.10 - (90.6 \pm 1.5)/2.3RT $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{\rm 8} {\rm H}_{\rm 8} \},M^{ - 1} {\rm s}^{ - 1} \} = 6.63 \pm 0.60 - (98.5 \pm 8.8)/2.3{\rm }\,RT $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{{\rm 10}} {\rm H}_{{\rm 10}} \},M^{ - 1} {\rm s}^{ - 1} \} = 8.27 \pm 0.66 - (143.3 \pm 9.8)/2.3RT $$\end{document} where the activation energies are in kJ/mol and the uncertainties are one standard deviation. As the reaction proceeds, the methyl indene and 1,2-dihydronaphthalene decompose, and indene and naphthalene are formed. In addition, an unidentified isomer of naphthalene is produced as an initial minor product, and it also decomposes as the reaction proceeds.
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  • 144
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    International Journal of Chemical Kinetics 19 (1987), S. 709-713 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of pyruvic acid into carbon dioxide and acetaldehyde is a unimolecular first-order reaction and takes place according to the rate equation, logk = 13.53-41,250/4.575 K. These parameters contrast markedly with those recently reported, viz. logk = 7.19-27,700/4.575 K and confirm that the latter, which gave an unacceptably low value for the frequency factor, are anomalous. The lower reactivity of pyruvic acid compared to oxalic acid is interpreted in terms of normal electronic effects.
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  • 145
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    International Journal of Chemical Kinetics 19 (1987), S. 715-724 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The static system decomposition kinetics of disilane (\documentclass{article}\pagestyle{empty}\begin{document}${\rm Si}_{\rm 2} {\rm H}_{\rm 6} \mathop {\longrightarrow}\limits^1 {\rm SiH}_{\rm 2} + {\rm SiH}_{\rm 4}$\end{document}, 538-587 K and 10-500 Torr), are reported. Reaction rate constants are weakly pressure dependent, and best fits of the data are realized with RRKM fall-off calculations using logA1,∞ = 15.75 and E1,∞ = 52,200 cal. These parameters yield AHf0(SiH2)298 = (63.5 - Eb, c) kcal mol,-1 where Eb, c is the activation energy for the back reaction at 550 K, M = 1 std state. Five other silylene heat-of-formation values (ranging from 63.9 - Eb, c to 66.0 - Eb, c kcal mol-1) are deduced from the reported decomposition kinetics of trisilane and methyldisilane, and from the reported absolute and relative rate constants for silylene insertions into H2 and SiH4. Assuming Eb, c = 0, an average value of ΔHf0(SiH2) = 64.3 ± 0.3 kcal mol-1 is obtained. Also, a recalculation of the activation energy for silylene insertion into H2, based in part on the new disilane decomposition Arrhenius parameters, gives (0.6 + Eb, c) kcal mol-1, in good agreement with theoretical calculations.
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    International Journal of Chemical Kinetics 19 (1987), S. 781-785 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 147
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 148
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    International Journal of Chemical Kinetics 19 (1987), S. 829-839 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 149
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    International Journal of Chemical Kinetics 19 (1987), S. 841-849 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to appreciate the excellent catalytic effect of iodine on the alcoholyses of alkoxysilanes more precisely, the rates of the reaction, Et3SiOBun + BusOH ⇌ Et3SiOBus + BunOH, were determined at various iodine concentrations.Both forward and reverse reactions are first order with respect to butoxysilane and to butanol, and pseudo first-order rate constants were measured at 40°, 30°, and 20°C on reaction mixtures containing both butanols in excess by means of gas-liquid chromatography. The observed rate constants as a function of iodine concentration gave linear relationships, and from these data the catalytic coefficients of iodine were evaluated: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {k_{2_{{\rm I}_2 } } = 7.4 \times 10^7 \exp (- 55.7 \times 10^3 /RT)} & {({\rm forward\, reaction})} \\ \end{array} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {k_{{ -2} _{{\rm I} _2 } } = 9.7 \times 10^7 \exp (- 54.3 \times 10^3 /RT)} & {({\rm reverse\, reaction})} \\ \end{array} $$\end{document} The enthalpies and the entropies of activation were estimated to be 53.2 kJ mol-1, -103 J K-1 mol-1 (forward, 30°C) and 51.8 kJ mol-1, minus;100 J K-1 mol-1 (reverse, 30°C).
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  • 150
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    International Journal of Chemical Kinetics 19 (1987), S. 851-867 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Values for 〈ΔEdown〉, the average downward energy transferred from the reactant to the bath gas upon collision, have been obtained for highly vibrationally excited undeuterated and per-deuterated isopropyl bromide with the bath gases Ne, Xe, C2H4, and C2D4, at ca. 870 K. The technique of pressure-dependent very low-pressure pyrolysis (VLPP) was used to obtain the data. For C3H7Br, the 〈ΔEdown〉 values (cm-1) are 490 (Ne), 540 (Xe), 820 (C2H4), and 740 (C2D4), and for C3D7Br, 440 (Ne), 570 (Xe), 730 (C2H4), and 810 (C2D4). The uncertainties in these values are ca. ±10%. The 〈ΔEdown〉 values for the inert bath gases Ne and Xe show excellent agreement with the theoretical predictions of the semi-empirical biased random walk model for monatomic/substrate collisional energy exchange [J. Chem. Phys., 80, 5501 (1984)]. The relative effects of deuteration of the reactant molecule on 〈ΔEdown〉 also compare favorably with the predictions of this theoretical model. Extrapolated high-pressure rate coefficients (s-1) for the thermal decomposition of reactant are 1013.6±0.3 exp(-200 ± 8 kJ mol-1/RT) for C3H7Br and 1013.9±0.3 exp(-207 ± 8 kJ mol±1/RT) for C3D7Br, which are consistent with previous studies and the expected isotope effect.
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    International Journal of Chemical Kinetics 19 (1987), S. 895-921 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: n-Hexyl and s-octyl radical isomerizations by intramolecular hydrogen atom shift have been studied in the presence of high methyl radical concentration where isomerized alkyl radicals reacted predominantly by combination and disproportionation reactions with methyl radicals.By assuming the rate coefficient of 1-hexyl radical recombination to be equal to that of ethyl self-combination, the rate coefficient of log(k1/s-1) = (9.5 ± 0.3) - (11.6 ± 0.3) kcal mol-1/RT ln 10 has been derived for the 6sp isomerization of n-hexyl radicals, 1-hexyl → 2-hexyl (1).Investigation of s-octyl radical isomerization was complicated by fast interconversion between 3-octyl, 2-octyl, and 4-octyl radicals. Use of the methyl trapping technique and systematic variation of methyl radical concentration made possible the determination of log(k2/s-1) = (9.4 ± 0.7) - (11.2 ± 1.0) kcal mol-1/RT ln 10 for the 6ss isomerization of 3-octyl and the estimation of log(k3/s-1) = 10.5-17 kcal mol-1/RT ln 10 for the 5ss isomerization of 2-octyl radicals, where 3-octyl → 2-octyl (2), and 2-octyl → 4-octyl (3).
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  • 152
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    International Journal of Chemical Kinetics 19 (1987) 
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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 19 (1987), S. 49-60 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of migration of acetyl, propionyl, isobutyryl, and benzoyl substituent in Diels-Alder adducts of acyl-1, 4-benzoquinones, (enediones), (I), to form the corresponding 2-acyl hydroquinones, (II), in 50% (v/v) ethanolic pyridine have been studied in detail. Rate dependence on pyridine concentration has been established and maximum rate was found at pyridine a volume percent of 25 in an ethanolic reaction mixture. The study indicated first-order dependence on reactants and fractional dependence on pyridine concentration. The effect of substituents of the acyl group on the rate showed that electronic factors play an important role on the stability of the transition state. A plausible mechanism, which is consistent with the results has been postulated and suitable rate law in consonance with the postulated mechanism have been derived.
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  • 154
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    International Journal of Chemical Kinetics 19 (1987), S. 61-79 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of acetonitrile was studied behind reflected shocks in a single pulse shock tube over the temperature range 1350-1950 K at overall densities of approximately 3 × 10-5 mol/cc. Methane and hydrogen cyanide are the major reaction products. They are formed by an attack of H and CH3 radicals on acetonitrile. The initiation step of the pyrolysis is the self dissociation of acetonitrile: for which the following rate constant was obtained: k1 = 6.17 × 1015exp(-96.6 × 103/RT)sec-1. Where R is given in units of cal/K mol. Additional reaction products which appear in the pyrolysis are: C2H2, C2H4, CH2=CHCN, CH≡CHCN, C2H5CN, C2N2, and C4H2. Acetylene is formed from methane pyrolysis and becomes a major reaction product at high temperatures. Acrilonitrile and cyanoacetylene are secondary products originating from the CH2CN radical. Rate parameters for the formation of the reaction products are given.
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  • 155
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    International Journal of Chemical Kinetics 19 (1987), S. 105-113 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solid solutions of Cu2O alone and Cu2O with ZnO or Cr2O3 in ZnO · Cr2O3 as well as solid solutions of ZnO in Cu2O · Cr2O3 have activities and selectivities for methanol synthesis comparable to solid solutions of Cu2O in ZnO. Addition of a secondary phase to these solid solutions limits the grain growth and produces higher surface areas.
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  • 156
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    International Journal of Chemical Kinetics 19 (1987), S. 81-103 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of n-hexane has been investigated in the ranges 723-823 K and 10-100 Torr at up to 3% decomposition. The reaction is homogeneous and free from the self-inhibition by olefin products observed for several other alkanes. The products of the reaction are hydrogen, methane, ethane, ethene, propene, but-1-ene, and pent-1-ene, with smaller amounts of propane. It is shown that the results are in quantitative agreement with a conventional Rice-Herzfeld chain mechanism terminated by the combination and disproportionation of ethyl radicals, but with the mechanism extended so as to include the unimolecular isomerizations via a six-membered cyclic transition state between 1-hexyl and 2-hexyl (1-methylpentyl) radicals.The overall rate constant of initiation is estimated to be given by \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}k_1 /{\rm s}^{ - {\rm 1}}) = 17.77 - (83.8\,{\rm kcal\, mol}^{ - {\rm 1}})/(2.3{\rm }RT) $$\end{document} The rate constant for the reaction is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ \log (k_9 /{\rm cm}^{\rm 3}\, {\rm mol}^{ - 1} {\rm s}^{ - 1}) = 13.30 - (17.9{\rm \, kcal\, mol}^{ - 1})/(2.3{\rm }\,RT) $$\end{document} which when combined with published data gives an Arrhenius plot curved upwards at low values of 1/T as has been observed for several other hydrogen abstraction reactions of methyl and of ethyl. Estimates are made of rate constants and ratios of rate constants for several reactions of the free radicals involved in the reaction. It is suggested that the minor product propane arises mainly from a hydrogen abstraction by 1-propyl from hexane with a contribution from a minor termination process involving ethyl and methyl.
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  • 157
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    International Journal of Chemical Kinetics 19 (1987), S. 115-128 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acetylperoxy radicals were produced by the flash photolysis of chlorine in the presence of acetaldehyde and oxygen. By adding various concentrations of nitrogen dioxide, the rate constant for the reaction producing PAN was measured to be k4 (153 Torr) = (2.29 ± 0.05) × 109 L/mol s.The effect of pressure has been studied over the range 76-612 Torr and the data fitted to a fall-off curve with k4∘ = 1.85 × 1013 L2/mol2 s. and k4x = 3.67 × 109 L/mol s. With a calculated value of the dissociation constant, k-4∘ = 268 L/mol s and of the equilibrium constant, K4 = 1.04 × 1012 L/mol, the expected strong collision value for k4∘ is 2.79 × 1014 L2/mol2 s.The ultraviolet absorption spectrum of PAN has been characterized in the range 205-260 nm.
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  • 158
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    International Journal of Chemical Kinetics 19 (1987), S. 129-142 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase chemical kinetics of SF4, SF5, and S2F10 are reviewed with particular emphasis on relevance to the general problem of the dielectric breakdown of SF6. Specific reaction systems treated are SF4 + F2, SF5 + SF5, and the pyrolysis of S2F10. Computer modeling calculations were carried out to arrive at the best estimates of rate parameters. Based on the results of these calculations, sets of recommended rate parameters are provided. The major discrepancies and problems in establishing the kinetic data base are described. Thermochemical consequences of different model calculations are given.
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  • 159
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    International Journal of Chemical Kinetics 19 (1987), S. 143-153 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aqueous cleavage of N-(2-bromoethyl)phthalimide (NBEPH), N-(3-bromopropyl)phthalimide (NBPPH), and N-carbethoxyphthalimide (NCPH) have been studied within the [ŌH] range of 5 × 10-4 M to 2 × 10-3 M, pH range of 8.82 to 10.62 and 8.06 to 8.66, respectively. The observed pseudo-first-order rate constants, kobs, reveal a linear relationship with [ŌH] with essentially zero intercept. The alkaline hydrolysis of N-(hydroxymethyl)phthalimide (NHMPH) has been studied within the [ŌH] range of 5.64 × 10-6 M to 2.0 M. The [OH]-rate profile reveals that both ionized and nonionized NHMPH are reactive toward ŌH. The second-order rate constant, kOH, for the reaction of ŌH with non-ionized NHMPH is ca. 104 times larger than that with ionized NHMPH. The values of kOH obtained for NBEPH, NBPPH, NCPH, and nonionized NHMPH show a reasonable linear relationship with Taft substituent constants, and the slope (ρ*) of the plot is 1.01 ± 0.10. The low value of ρ* of 1.01 is attributed to nucleophilic attack as the rate-limiting. The kOH value for ionized NHMPH reveals nearly 103-fold negative deviation from the linear Taft plot.
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  • 160
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  • 161
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    International Journal of Chemical Kinetics 19 (1987), S. 155-170 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic reinvestigation of the title redox system in aqueous alkaline media at 35°C and an ionic strength of 0.5 mol dm-3 shows that the reaction follows a pseudosecond-order Fe(CN)63- disappearance. While varying [phenol]0 and [OH-] exhibit a linear influence on the pseudo-second-order rate constant, varying[Fe(CN)63-]0 and [Fe(CN)64-]0, initially taken, have a complicated inhibitory effect on the same. The major phenoloxidation products isolated under a chosen condition are 2,2′- and 4,4′- dihydroxydiphenyl. Results are interpreted in terms of a probable mechanism which envisages a reversible formation, by the first one-electron transfer, of a reactive phenoxy radical (PhO·) which on the second one-electron transfer forms a less reactive ion-pair intermediate (stabilized by the Fe(CN)64- produced) to decompose rate-determiningly to phenoxonium cation (PhO+) and Fe(CN)64-, the product-formation steps being very rapid and kinetically indistinguishable.
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  • 162
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    International Journal of Chemical Kinetics 19 (1987), S. 277-298 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics and mechanism of the cerium(IV) oxidation of Cr(III) complexes of a series of macrocyclic (or pseudomacrocyclic) ligands with [14]-membered intraligand ring-sizes have now been investigated at I = 1.0 M (LiClO4) Temp. 30°C. The complexes of the formulation Cr(macrocycle)(X)(H2O)(3-n)+ where X = CHCl2 and H2O, n = 0 or 1 undergo oxidation to Cr(VI) with the formation of chromium(IV) intermediates. The observed kinetic parameters for the Ce(IV) oxidation of Cr(III) macrocyclic complexes have been discussed in terms of changes brought about by the macrocyclic ligands on the Cr(III) - Cr(IV) redox potentials and in specific rates for Cr(IV) - Cr(V) conversion. On the basis of this study, it has been suggested that the trapping of Cr(IV) is easier when a macrocyclic ligand having a symmetrical intra-ligand ring size and unsaturation in the cyclic structure is coordinated equatorially. Cyclic voltammetric studies indicate the formation of Cr(IV) transient in the case of electrochemical oxidation of trans-Cr(Me4[14]tetraene)(H2O)23+.
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  • 163
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    International Journal of Chemical Kinetics 19 (1987), S. 309-317 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Absolute rate constants have been measured for the reactions of trichloromethylperoxyl radicals with cyclohexane, cyclohexene, and hexamethylbenzene. The CCl3O2 radicals were produced by pulse radiolysis of air-saturated CCl4 solutions containing various amounts of the hydrocarbons. The rate constants were determined by competition with the one-electron oxidation of metalloporphyrins, using the rate of formation of the metalloporphyrin radical cation absorption to monitor the reaction by kinetic spectrophotometry. The rate constants for hydrogen abstraction from cyclohexane, cyclohexene, and hexamethylbenzene were found to be 1 × 103, 1.0 × 105, and 7.5 × 104 M-1 s-1, respectively.
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  • 164
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    International Journal of Chemical Kinetics 19 (1987), S. 975-996 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of acetylene has been studied in the temperature and pressure regimes of 1900-2500 K and 0.3-0.55 atm using a shock tube coupled to a time-of-flight mass spectrometer. A series of mixtures varying from 1.0-6.2% C2H2 diluted in a Ne-Ar mixture yielded a carbon atom density range of 0.24-2.0 × 1017 atoms cm-3 in the reflected shock zone. Concentration profiles for C2H2, C4H2, and C6H2 were constructed during typical observation times of 750 μs. C8H2 and trace amounts of C4H3 were found in relatively low concentrations at the high-temperature end of this study. A mechanism for acetylene pyrolysis is proposed, which successfully models this work and the results obtained by several other groups employing a variety of analytical techniques. Two values of the heat of formation for C2H(134 ± 2 and 127 ± 1 kcal/mol) were employed in the modeling process; superior fits to the data were attained using the latter value. The initial step of acetylene decomposition involves competition between two channels. In mixtures (〈200 ppm) where the acetylene concentrations are less than 2.18 × 10-9 mol cm-3, the decay is predominantly first order with respect to C2H2; in mixtures 〉200 ppm, the dominant initial step is second order. The rate constant for the second-order reaction is described by the equation \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2 \times 10^{13} \exp\, {\rm }(- 44.5{\rm\, kcal/}RT){\rm cm}^{\rm 3}\, {\rm mol}^{{\rm - 1}} {\rm s}^{{\rm - 1}} $$\end{document}Benzene concentrations predicted by the model are below the TOF detectability limit. C4H3 was observed in the 6.2% C2H2 mixture in accordance with the proposed mechanism.
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  • 165
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    International Journal of Chemical Kinetics 19 (1987), S. 1063-1072 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the Diels-Alder additions of CH2 — CHCHO, CH2—C(CH3)CHO, and CH2—CHC(CH3)O to cyclohexa-1,3-diene (CHD) have been studied in the gas phase. The stereochemistry and the mechanism of these reactions are discussed. In contrast with other Diels-Alder additions involving CHD as diene, a biradical mechanism does not fit the experimental results.
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  • 166
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    International Journal of Chemical Kinetics 19 (1987), S. 415-434 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aqueous cleavage of methyl salicylate has been studied in the buffer solutions of various primary mono- and di-amines as well as secondary amines at 30°C. Both ionized (MS-) and nonionized (MSH) methyl salicylate are reactive toward primary mono- and di-amines. The second-order rate constants for the reactions of MS- with primary mono- and di-amines of pKa 〉 9.4 exhibit Bronsted plot of slope (βnuc) of 0.82. This high value of βnuc is attributed to an intramolecular proton transfer in a thermodynamically unfavorable direction in the rate-determining step in a stepwise process for the formation of monoanionic tetrahedral intermediate. However, a concerted process for the formation of a monoanionic tetrahedral intermediate in the reactions of MS- with amine nucleophiles wherein expulsion of leaving group is a rate-determining step is not completely ruled out. The α-effect nitrogen nucleophiles hydroxylamine and hydrazine reveal, respectively, ca. 104- and 103-fold higher reactivity compared to other amine nucleophiles of comparable basicity. The value of βnuc of 1.03 obtained for the reactions of primary monoamines with MSH is ascribed to the expulsion of leaving group as the rate-determining step. The significantly lower value of βnuc of 0.60 obtained in the reactions of MSH with both monoprotonated and unprotonated diamines is explained in terms of possible occurrence of intramolecular general acid-base catalysis. Intramolecular general base catalysis is responsible for the enhanced nucleophilic reactivity of primary amines toward MS-. Dimethylamine, piperidine, morpholine, and piperazine have no detectable nucleophilic reactivity toward MS-.
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  • 167
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  • 168
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    International Journal of Chemical Kinetics 19 (1987), S. 1073-1082 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants of the gas phase reaction of OH radicals with dimethyl sulfide (CH3SCH3) over the temperature range 260-393 K have been studied using the discharge flow-resonance fluorescence technique. The rate constants were fitted by the Arrhenius equation k = (11.8 ± 2.2) × 10-12 exp[-(236 ± 150)/T] cm3 molecule-1 s-1 with k = (5.5 ± 1.0) × 10-12 cm3 molecule-1 s-1 at 298 K. Our results are in good agreement with the lower range of values reported previously. The observation of a small positive activation energy agrees well with that reported by Hynes et al. The rate constant was not affected by the total pressure variation (0.8-3.0 torr) or by the addition of oxygen (up to 1 torr) in the flow tube.
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  • 169
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    International Journal of Chemical Kinetics 19 (1987), S. 1107-1107 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Br atoms produced in a microwave discharge react abnormally rapidly with isobutane to produce HBr + t-Butyl. A VLPR study of the system at high Br atom concentration (Br ˜ 1013/cc) between 298 and 363 K permits one to separate the effects of excited atoms, Br* (2P1/2) from ground state atoms, Br (2P3/2). Rate constants for the latter agree well with bromination measurements and permit fixing ΔHƒ2980(tBu) at 9.5 ± 0.5kcal/mol in agreement with earlier work.
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  • 170
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    International Journal of Chemical Kinetics 19 (1987), S. 319-362 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experimental data for the reaction of O atoms with NH3 have been reviewed with particular attention to the possible effects of secondary reactions on the deduced rate coefficient. A reaction mechanism was assembled and computer calculations carried out to simulate several sets of experiments. The sensitivity of the calculations to uncertainties in the various rate coefficients was assessed. Transition-state theory calculations were carried out on the rate coefficient k1 for the O + NH3 → OH + NH2 reaction. These studies suggest that the reaction stoichiometry is dependent on temperature, initial reagent ratios, and extent of reaction; that available data are not sufficient to determine whether the initial step is H-atom abstraction (producing OH and NH2 radicals) or O-atom addition (producing an NH3O* complex): and that the low temperature values of k1 (T ≤ 400 K) are not consistent with values deduced at higher temperatures if the reaction proceeds by H-atom abstraction. Taking all the evidence into account, it is recommended that the expression 1.1 × 103 T2.1 exp(-2620/T) L mol-1 s-1 be used for k1 until more definitive experimental measurements are made at low temperatures.
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  • 171
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    International Journal of Chemical Kinetics 19 (1987), S. 391-400 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By allowing the t-butoxy radical to decompose in the presence of nitric oxide, it has been possible to determine rate constants for decomposition by the measurements of the relative rates (2) and (3) Process (3) is clearly pressure dependent. The value of k3(∞) has been determined in the presence of several inert gases (CF4, SF6, N2, and Ar) and a value of k3 interpolated for atmospheric conditions. The results may be compared with those for other relevant alkoxy radicals at room temperature. Extrapolated values for k3 in the presence of CF4 lead to the result \documentclass{article}\pagestyle{empty}\begin{document}$$ k_3 (\infty)/s^{ - 1} = 10^{14.6 \pm 0.6} \exp (- 8052 \pm 604/T) $$\end{document}
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    International Journal of Chemical Kinetics 19 (1987), S. 401-413 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Disproportionation-combination rate constant ratios, kd/kc, have been determined for R + RCH2CHCl and for the auto disproportionation-combination of RCH2CHCl radicals, R = CF3, C2F5, and C3F7. The kd/kc for R = CF3 and to a lesser degree for R = C2F5 and C3F7 were very sensitive to the surface/volume ratio of the reaction vessel suggesting a heterogeneous component for disproportionation.
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    International Journal of Chemical Kinetics 19 (1987), S. 373-389 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The average downward energy transfer (〈Δ Edown〉) is obtained for highly vibrationally excited acetyl chloride with Ne and C2H4 bath gases at ca. 870 K. Data are obtained by the technique of very low-pressure pyrolysis (VLPP). Fitting these data by solution of the appropriate reaction-diffusion integrodifferential master equation yields the gas/gas collisional energy transfer parameters: 〈Δ Edown〉 values are 220 ± 10 cm-1 (Ne bath gas) and 330 ± 20 cm-1 (C2H4).These energy transfer quantities are much less than those predicted by statistical theories, or those observed for similar sized molecules such as CH3CH2Cl. These results are explained by the qualitative predictions of the biased random walk model wherein the fundamental mechanism of energy transfer is the multiple interactions between the bath gas and the individual atoms of the reactant molecule, during the course of the collision event. The charge distribution of acetyl chloride decreases the number of such interactions, thereby reducing the amount of energy transferred per collision.
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    International Journal of Chemical Kinetics 19 (1987), S. 487-487 
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    Keywords: Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology
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  • 176
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  • 177
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    International Journal of Chemical Kinetics 19 (1987), S. 489-501 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A steady-state system involving the photolysis of NO2 in an excess of I2 as a source of IO radicals has been used to study the reaction IO + DMS in 760 Torr N2 at 296 K. IO radicals were found to react rapidly with DMS, one molecule of DMSO being produced for each molecule of DMS consumed. Numerical analysis of the experimental results yielded a rate constant of (3.0 ± 1.5) × 10-11 cm3 s-1 for the reaction IO + DMS → DMSO + I.
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    International Journal of Chemical Kinetics 19 (1987), S. 513-518 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rates of acidic hydrolysis of hexano-, octano-, and decanohydroxamic acids and of 4-bromophenylaceto- and phenylacetohydroxamic acids have been determined in aqueous perfluorooctanoic acid - a reactive counterion surfactant system. Typical micellar catalysis was observed for the hydrolyses of the n-alkyl hydroxamic acids but not for the arylacetohydroxamic acids. The Arrhenius activation energy for hydrolysis of octano-hydroxamic acid is smaller above the cmc of the surfactant than it is below the cmc.
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    International Journal of Chemical Kinetics 19 (1987), S. 519-537 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the direct synthesis reaction (Si + 2CH3Cl → (CH3)2SiCl2) were measured on a Cu3Si alloy containing 1.2 atom % Zn. Reaction was carried out in a differential reactor (520-595 K, 1 atm) attached to an ultrahigh vacuum (UHV) system. Auger spectroscopy was used to characterize the surface before and after reaction. Zinc does not significantly change the overall rate of reaction, but it changes selectivity to dimethyldichlorosilane (the desired product), surface composition, activation energies, and induction times. The rate of silicon diffusion to the surface is not limiting in the presence of zinc. Zinc is found to be a promoter for improved selectivity only in low concentrations, and only a fraction of the surface appears to be active for reaction. The kinetics appear relatively insensitive to the surface composition or the form of surface carbon. A Cu3Si surface with Zn is shown to be a good model catalyst for the direct synthesis reaction.
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  • 180
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    International Journal of Chemical Kinetics 19 (1987), S. 553-570 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We examine the kinetic model D. The differential equations describing this reaction scheme are cast in a nondimensional form and analyzed in four basic approximation regimes: a ‘pseudo-first order’ approximation valid for small values of the ratio of the initial concentrations of the reactants; an asymptotic solution valid for large values of k3; the standard steady state (Bodenstein) approximation; and an approximation to a second order system without intermediate. Interconnecting relationships between the various approximations derived are examined, and the approximations are compared to numerical solutions to the full equations. The results are assessed from the standpoint of the experimental kineticist, and it is suggested that the reaction studied, and consequently many other more complex reactions, may under certain circumstances be subject to non-unique interpretation.
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  • 181
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    International Journal of Chemical Kinetics 19 (1987), S. 609-614 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of decay of ozone in a large excess of the cycloalkene have been re-measured by an improved experimental procedure, and the following second-order rate constants (cm3 molecule-1 s-1) have been determined in synthetic air at atmospheric pressure: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm O}_3 + {\rm cyclopentene} \longrightarrow {\rm products,}} & {k = (4.97 \pm 0.30) \times 10^{ - 16} {\rm at}} \\ \end{array}291.5{\rm K} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {{\rm O}_3 + {\rm cyclohexene} \longrightarrow {\rm products,}} & {k = (1.51 \pm 0.10) \times 10^{ - 16} {\rm at}} \\ \end{array}295{\rm K} $$\end{document} The results are discussed in relation to existing literature data on the kinetics of ozonecycloalkene reactions.
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  • 182
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    International Journal of Chemical Kinetics 19 (1987), S. 539-551 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The surface reaction of NO2 and H2O vapor to emit HONO into the gas phase was studied in the evacuable and bakeable photochemical chamber under the irradiation of UV-visible light (≳ 290 nm). Kinetic analysis of the NO, NO2, and HONO with the aid of computer modeling strongly suggested that the formation of HONO by the surface reaction is photoenhanced. When a linear regression was assumed, the photoenhancement factor defined by {(k′21/k21) - 1} was expressed as (6.8 ± 2.5)k1 under our experimental conditions, where k1 is the primary photolysis rate of NO2, and k21, k′21 are the second-order-equivalent rate constants of the HONO formation reaction in dark and under irradiation, respectively. The discussion was made that this photocatalitic enhancement of HONO formation would explain the nature of the extra OH radical flux in the smog chamber experiments, which has been discussed as “unknown radical source” and has still been unexplained by the surface dark reaction of NO2 and H2O to emit HONO.
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  • 183
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 184
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The following gas-phase reactions: were studied by the competitive method with CF3I as the source of radicals. The kinetic parameters obtained in the temperature range 533-613 K and 503-613 K respectively for chlorine atom transfer reactions are given by: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k_1 /k_c ^{1/2} ({\rm cm}^{\rm 3}\, {\rm mol}^{{\rm - 1/2}} s^{ - 1/2}) = (6.19 \pm 0.10) - (16900 \pm 100)/\theta $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k_2 /k_c ^{1/2} ({\rm cm}^{\rm 3}\, {\rm mol}^{{\rm - 1/2}} s^{ - 1/2}) = (6.52 \pm 0.10) - (14890 \pm 100)/\theta $$\end{document} where θ = 2.303 RT (cal mol-1).The Arrhenius A values were calculated for seven chlorine atom transfer reactions (CF2Cl2, CFCl3, CCl4 with CF3 radicals; CF3Cl, CF2Cl2, CFCl3 and CCl4 with CH3 radicals) by using the thermochemical kinetic version of the Transition State Theory (TST).
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  • 185
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    International Journal of Chemical Kinetics 19 (1987), S. 649-658 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Published data show that in its early stages (up to 3% decomposition), the pyrolysis of n-hexane in the ranges 723-823 K and 10-100 Torr is not inhibited by the olefin products, in contrast with neopentane pyrolysis which is very strongly inhibited in similar conditions. Detailed consideration of the chain mechanisms for the two pyrolyses shows that the reactivity of the chain terminating radical towards hydrogen abstraction from an allylic C—H bond in product olefin is the factor which determines whether or not observable self-inhibition occurs. Thus, n-hexane pyrolysis, whose chain decomposition is terminated by recombination and disproportionation of ethyl, is not significantly self-inhibited, whereas that of neopentane which is terminated by recombination of methyl is very strongly inhibited because methyl is 14× more reactive than ethyl. The implications for other alkanes are briefly discussed.
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  • 186
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    International Journal of Chemical Kinetics 19 (1987), S. 683-690 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase elimination of 4-(methylthio)-1-butyl acetate and 1-chloro-4-(methylthio)-butane has been investigated in a seasoned, static reaction vessel over the temperature range of 310-410°C and the pressure range of 46-193 Torr. The presence of the inhibitors propene, cyclohexene, and/or toluene had no effect on the rates. The reactions are homogeneous, unimolecular, and obey a first-order rate law. The rate coefficients are given by the following Arrhenius equations: for 4-(methylthio)-1-butyl acetate, log k1(s-1) = (12.32 ± 0.29) - (192.1 ± 3.6) kJ/mol/2.303RT; for 1-chloro-4-(methylthio)-butane, log k1(s-1) = (12.23 ± 0.59) - (175.7 ± 6.8) kJ/mol/2.303RT. The CH3S substituent in 1-chloro-4-(methylthio)-butane has been found to participate in the elimination reaction, where tetrahydrothiophene and methyl chloride formation may result from an intimate ion-pair type of mechanism. The yield of a cyclic product in gas phase reactions provides additional evidence of an intimate ion pair mechanism through neighboring group participation in gas phase elimination of special types of organic halides.
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  • 187
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    International Journal of Chemical Kinetics 19 (1987), S. 741-755 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the permanganate oxidation of formic acid in aqueous perchloric acid at 30°C were examined by the spectrophotometric method. The chemical reaction 2MnO4- + 3HCOOH + 2H+ → 2MnO2 + 3CO2 + 4H2O, appears to proceed via several parallel reactions. The overall rate equation has been obtained by using statistical multilinear regression analysis of the 660 cases studied, and the presence in the rate equation of two new terms in relation to previous studies shows that both permanganate autocatalytic effects and acid media inhibition must be taken into account when the reaction proceeds at constant ionic strength.
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  • 188
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    International Journal of Chemical Kinetics 19 (1987), S. 777-780 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 189
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    International Journal of Chemical Kinetics 19 (1987), S. 799-828 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A previous technique for the calculation of rate constants for the gas-phase reactions of the OH radical with organic compounds has been updated and extended to include sulfur- and nitrogen-containing compounds. The overall OH radical reaction rate constants are separated into individual processes involving (a) H-atom abstraction from C—H and O—H bonds in saturated organics, (b) OH radical addition to 〉C=C〈 and —C≡C— unsaturated bonds, (c) OH radical addition to aromatic rings, and (d) OH radical interaction with —NH2, 〉NH, 〉N—, —SH, and —S— groups. During its development, this estimation technique has been tested against the available database, and only for 18 out of a total of ca. 300 organic compounds do the calculated and experimental room temperature rate constants disagree by more than a factor of 2. This suggests that this technique has utility in estimating OH radical reaction rate constants at room temperature and atmospheric pressure of air, and hence atmospheric lifetimes due to OH radical reaction, for organic compounds for which experimental data are not available. In addition, OH radical reaction rate constants can be estimated over the temperature range ca. 250-1000 K for those organic compounds which react via H-atom abstraction from C—H and O—H bonds, and over the temperature range ca. 250-500 K for compounds containing 〉C=C〈 bond systems.
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  • 190
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    Keywords: Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology
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  • 191
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    International Journal of Chemical Kinetics 19 (1987), S. 929-942 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constant of the primary decomposition step was determined for four symmetrical and four unsymmetrical azoalkanes. From the experimental activation energies and some literature enthalpy data, the following enthalpies of formation of radicals and group contributions were calculated: ΔHƒ (CH3N2) = 51.5 ± 1.8 kcal mol-1, ΔHƒ (C2H5N2) = 44.8 ± 2.5 kcal mol-1, ΔHƒ (2-C3H7N2) = 37.9 ± 2.2 kcal mol-1, [NA-(C)] = 27.6 ± 3.7 kcal mol-1, [NA-(ṄA) (C)] = 61.2 ± 3.1 kcal mol-1.
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  • 192
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 193
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    International Journal of Chemical Kinetics 19 (1987), S. 963-973 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new determination of the disproportionation/combination ratio for C2F5 and C2H5 radicals gives a value of Δ(C2F5, C2H5) = 0.24 ± 0.02, independent of temperature. The cross-combination ratio for the two radicals was found to increase with temperature and the significance of this is discussed in evaluating Δ.
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  • 194
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    International Journal of Chemical Kinetics 19 (1987), S. 1015-1023 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of aliphatic alcohols using the flash photolysis resonance fluorescence technique. Experiments were performed over the temperature range 240-440 K at total pressures (using Ar diluent gas) between 25-50 Torr. The kinetic data for methanol (k1), ethanol (k2), and 2-propanol (k3) were used to derive the Arrhenius expressions \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = (4.8 \pm 1.2) \times 10^{ - 12} \exp [- (480 \pm 70)/T]\,{\rm cm}^3\, {\rm molecule}^{ - 1} {\rm s}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_2 = (7.4 \pm 3.2) \times 10^{ - 12} \exp [- (240 \pm 110)/T]{\rm cm}^3 {\rm molecule}^{ - 1} {\rm s}^{ - 1} $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$ k_3 = (5.8 \pm 1.9) \times 10^{ - 12} \exp [- (30 \pm 90)/T]\,{\rm cm}^3\, {\rm molecule}^{ - 1} {\rm s}^{ - 1} $$\end{document} At 296 K, the measured rate constants (in units of 10-13 cm3 molecule-1 s-1) were: k1 = (8.61 ± 0.47), k2 = (33.3 ± 2.3), and k3 = (58.1 ± 3.4). Room temperature rate constants for the OH reactions with several other aliphatic alcohols were also measured. These were (in the above units): 1-propanol, (53.4 ± 2.9); 1-butanol, (83.1 ± 6.3) and 1-pentanol, (108 ± 11). The results are discussed in terms of the mechanisms for these reactions and are compared to previous literature data.
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  • 195
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    International Journal of Chemical Kinetics 19 (1987), S. 1025-1047 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of ligand substitution in 17- and 19-electron organometallic radicals is discussed. These species substitute ligands by an associative process some 106 to 1010 faster than analogous 18-electron complexes. When 17-electron species can be generated by bond homolysis or electron transfer reactions of 18-electron complexes, they can act as intermediates in radical chain reactions of 18-electron complexes. A 17-19 electron rule is proposed to explain transformations of organometallic radicals just as the 16-18 electron rule finds use for closed shell organometallic complexes. The origin of this rule is the favorable two-center three-electron bond that can form when an odd electron in a sterically accessible metal d-orbital interacts with an electron pair on an entering nucleophile. Besides simple substitution, these radicals can disproportionate, dimerize, and undergo insertion or atom abstraction reactions.
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  • 196
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    International Journal of Chemical Kinetics 19 (1987), S. 171-181 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed statistical study is presented, based on simulated experimental data, on the estimation of activation parameters using the Arrhenius equation: k = A exp(B/T). The close correlation of the two parameters is shown, which requires the computation of the covariance matrix for the representation of uncertainties. This matrix facilitates the correct estimation of the confidence interval for interpolated (or extrapolated) values of rate coefficients. It is proposed that the full correlation matrix should be published in any article dealing with the determination of Arrhenius parameters.The importance of correct weighting is emphasized. Nonlinear fitting to the Arrhenius equation can be carried out without weighting only in case the (absolute) error of rate coefficient is independent of the temperature. Simulated experiments show that noncorrect weighting shifts the average values of fitted parameters and increases the variance of the parameters as well.With respect to the modified Arrhenius equation: k = A · Tn exp(B/T), statistical analysis shows that the physically meaningful estimation of all three parameters is impossible. Nonlinear fitting of three parameters is suggested for interpolation (and extrapolation) of rate coefficients, whereas in case of activation parameter estimation, the fixing of “n” on the basis of theoretical considerations is advised followed by the estimation of the remaining two parameters.
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  • 197
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    International Journal of Chemical Kinetics 19 (1987), S. 183-189 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of 4-chloro-1-butanol has been studied in a static system, seasoned with allyl bromide, and in the presence of the free radical suppressor toluene. The working temperature and pressure ranges were 400-450°C and 43-164 Torr, respectively. The reaction is homogeneous, unimolecular, and follows a first-order rate law. The temperature dependence of the rate coefficients is given by the following Arrhenius equation: log k1(s-1) = (13.34 ± 0.50) - (221.1 ± 6.7) kJ mol-1 (2.303RT)-1. The products tetrahydrofuran, formaldehyde, and propene, arise by the participation of the neighboring OH group in 4-chloro-1-butanol pyrolysis. The reaction is best explained in terms of an intimate ion pair type of mechanism.
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  • 198
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    International Journal of Chemical Kinetics 19 (1987), S. 191-205 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase reaction of N2O5 with water vapor was investigated in a 17.3-m3 Teflon lined chamber. Temporal concentration profiles for ozone, total nitrogen oxides, and nitrogen dioxide were measured. Concentration profiles for N2O5 and HNO3 were calculated from a combination of measurements of nitrogenous species. A kinetic mechanism with an adjustable value for the rate constant of N2O5 + H2O was used to model the experiments. From this analysis an upper limit value of k ≤ 4 × 10-7 ppm-1 min-1 for the gas phase reaction N2O5 + H2O → 2HNO3 was derived.
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  • 199
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    International Journal of Chemical Kinetics 19 (1987), S. 207-228 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions which proceed through energized adducts, including radical recombinations, insertions, and addition to unsaturates, frequently exhibit unusual kinetic behavior. The branching ratios among various product channels are often complex functions of both temperature and pressure. Four such reactions involving methyl radicals are analyzed by combining chemical activation distribution functions with QRRK methods to predict rate constants for each channel. These include three oxidation paths, CH3 + O, CH3 + O2, CH3 + OH, and the addition reaction CH3 + C2H2. These predictions are compared to experiments wherever possible; generally, the agreement is quite satisfactory. Analysis of the energetics of the various reaction channels, using parameters which are readily available, provides a convenient framework for prediction. Suggested rate constants for the various channels for the four reactions are given at three pressures, 20, 760, and 7600 Torr, for the temperature range 300-2500 K. The approach used here can easily be applied to other reactions.
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  • 200
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    International Journal of Chemical Kinetics 19 (1987), S. 229-242 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The direct photolysis of bicyclo[4.2.0]octa-2,4-diene in the gas phase at 280-300 nm produces mainly 1,3,5-cyclooctatriene and benzene plus ethylene. The yield of the former product is enhanced by added gases, and it is proposed that it is formed in a vibrationally excited state which can revert to bicyclooctadiene unless the excess energy is removed in collisions. Computer modelling of the direct photolysis yielded quantitative agreement with the experimental results, but only when large, arbitrary adjustments were made to the calculated rate constants for the interconversion of cyclooctratriene and bicyclooctadiene. The Hg(63P1) sensitized reaction of bicyclooctadiene produces mainly benzene plus ethylene, a process which is also enhanced by added gases.
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