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  • 1985-1989  (137)
  • 1935-1939
  • 1988  (137)
  • Physical Chemistry  (137)
  • 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
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    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
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    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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    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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    New York, NY : Wiley-Blackwell
    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.
    Additional Material: 3 Ill.
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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.
    Additional Material: 5 Ill.
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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).
    Additional Material: 5 Ill.
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  • 131
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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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  • 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.
    Additional Material: 9 Ill.
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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
    Type of Medium: Electronic Resource
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  • 135
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    New York, NY : Wiley-Blackwell
    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.
    Additional Material: 4 Ill.
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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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    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
    Type of Medium: Electronic Resource
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