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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 431-436 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Imidazole (Imz)-catalysed hydrolysis of benzoate esters proceeds via the intermediate formation of N-benzoylimidazoles. This paper considers the second step of this reaction, viz., Imz-catalysed hydrolysis of N-(4-X-benzoyl)imidazoles, X = CH3, H, Cl, CN and NO2, and N-(disubstituted benzoyl)imidazoles, 2-chloro-4-nitro, 2, 4-dinitro and 3,5-dinitro, in water-acetonitrile mixtures (10% or 14%, v/v, in organic solvent). On the basis of catalytic rate constants and the kinetic solvent isotope effect, it is shown that catalysis by Imz is of the general-base type. Unexpectedly, the hydrolysis of N-(2,4-dinitrobenzoyl)imidazole was found to be slower than that of N-(4-nitrobenzoyl)imidazole. It is shown that this reactivity order is due to a combination of a steric effect and stabilization of the reactant state due to a donor-acceptor interaction between the Imz moiety and the 2,4-dinitrophenyl ring.
    Additional Material: 2 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 435-441 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ring proton affinities (PAs) in fluorobenzene and toluene were examined by the MP2(fc)/6-31G**//HF/6-31G* + ZPE(HF/6-31G*) model. The calculated PAs are in good accordance with the available experimental evidence, their order being PA(p) 〉 PA(o) 〉 PA(m) 〉 PA(i), where p, o, m and i stand for para, ortho, meta and ipso positions, respectively. The relative values of the proton affinities can be interpreted in terms of the ground-state charge distribution (initial state effect) and the characteristic π-bond fixation produced by protonation (final state effect). The influence of the latter is either concerted with the initial charge distribution leading to higher PAs (ortho and para positions) or disconcerted as in meta protonation, which has a lower PA value. Finally, it is shown that PAs in difluorobenzenes and fluorotoluenes are additive and can be reduced to the characteristic PAs of fluorobenzene and toluene with good accuracy.
    Additional Material: 3 Tab.
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The activation energy parameters for the reaction of PdX42- (X=Cl-, Br-) in aqueous halide acid solution with thiourea (tu) and selenourea (seu) have been determined. High rates of reaction parallel low enthalpies and appreciable negative entropy of activation. The rate law in each case simplifies to kobs=k[L] where L=tu or seu, and only ligand-dependent rate constants are observed at 25°C. The ligand-dependent rate constants for the first identifiable step in the PdCl42- + X system is (9.1±0.1) × 103 M-1 sec-1 and (4.5±0.1) × 104 M-1 sec-1 for X=tu and seu, respectively, while for the PdBr42- + X system it is (2.0±0.1) × 104 M-1 sec-1 and (9.0±0.1) × 104 M-1 sec-1 for X=tu and seu, respectively.
    Additional Material: 4 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 725-739 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants of change transfer reactions kCT, involving C3—C9 alkanes and cycloalkanes, have been determined in an ion cyclotron resonance mass spectrometer. The rate constants are significantly lower than the corresponding rate constants for collision when the reaction is less than about 0.5 eV exothermic for linear alkane ions, or less than about 0.2 eV exothermic for cycloalkane ions. In this region of low reaction efficiency, the efficiency of reaction with linear or branched alkanes seems to depend primarily on reaction exothermicity. (The efficiencies of reaction of a given ion with cyclic alkanes also depend on ΔHrn, but are higher than for reactions with other compounds). Although the lowered reaction efficiencies probably result, at least in part, from unfavorable Franck-Condon factors in the energy range near the ionization onset, quantitative correlations between reaction efficiency and estimated relative Franck-Condon factors were not observed. When the enthalpy of reaction is small (less than about -0.15 eV), it is seen that the reverse charge transfer can also occur, and equilibrium is established under the conditions of these experiments. From the observed equilibrium constants, values for the standard free energy change are derived, and assuming that ΔS is small for electron transfer equilibria, values of ΔHrn are estimated. In the case of the equilibria involving cyclohexane ion, these values of ΔHrn lead to estimates of the ionization potentials of methylcyclopentane, 3-methylpentane, n-octane, 2,2-dimethylbutane, and 2,3-dimethylbutane, which are lower than the ionization potentials of cyclohexane, that is, 〈9.88 eV, although all these compounds had previously been reported to have ionization potentials above 10.03 eV. That the ionization potentials are indeed lower than 10.03 eV is confirmed by determining the quantum yields of ionization with 10.03-eV photons.It is pointed out that the conclusions reached here apparently also apply to the charge transfer reactions of alkane ions in the liquid phase.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 18 (1986), S. 1315-1321 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Trichloromethylperoxyl radicals were produced by pulse radiolysis of air saturated solutions containing CCl4. The rate constants for the reaction of CCl3O2 radicals with zinc tetraphenylporphyrin (ZnTPP) were determined in various solvents. They were found to vary between 3 × 107 and 3 × 109 M-1 s-1. The changes in rate constants result from complexation of ZnTPP with the different solvents, but did not correspond to changes in redox potential of ZnTPP. The rate constants were found to depend on the strength of the axial complexation, indicating an inner sphere mechanism whereby the radical binds to the metal prior to electron transfer.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 387-397 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition of 1-chloro-1,1-difluoroethane by a radical chain reaction has been studied in a flow reactor in the temperature range from 503 to 773 K. For the initiation of the chain small amounts of added chlorine were photolyzed with a XeCl laser (λ = 308 nm). The formation of the dehydrochlorination and chlorination products, vinylidene fluoride, and 1,2-dichloro-1,1-difluoroethane respectively, is described by a kinetic model. Arrhenius parameters for the two abstraction reactions \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CI + CH}_{\rm 3} {\rm CCIF}_{\rm 2} {\hbox to 25pt{\rightarrowfill}} {\hskip-18pt ^{K_2 }}{\hskip1em} {\rm HCI + CH}_{\rm 2} {\rm CCIF}_{\rm 2}$$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CI + CH}_{\rm 2} {\rm CICCIF}_{\rm 2} {\hbox to 25pt{\rightarrowfill}} {\hskip-18pt ^{K_7 }}{\hskip1em} {\rm HCI + CHCICCIF}_{\rm 2}$$\end{document} were determined by a competition method: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} (k_2 /cm^3 {\rm mol}^{{\rm - 1}} {\rm s}^{{\rm - 1}} = (13.6 \pm 0.1) - (9200 \pm 300)/4.576T$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} (k_7 /cm^3 {\rm mol}^{{\rm - 1}} {\rm s}^{{\rm - 1}} = (13.7 \pm 0.1) - (6500 \pm 200)/4.576T$$\end{document} Experimental and modeling results are discussed with respect to former studies on the thermal reaction of 1-chloro-1,1-difluoroethane.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 181-188 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser flash photolysis (at 248 or 308 nm) or aryl iodides in water or water/methanol solutions produces iodine atoms and phenyl radicals. Iodine atoms react rapidly with added I- to form I2- but do not react rapidly with O2 (k ≤ 107 L mol-1 s-1). Iodine atoms oxidize phenols to phenoxyl radicals, with rate constants that vary from 1.6 × 107 L mol-1 s-1 for phenol to about 6 × 109 L mol-1 s-1 for 4-methoxyphenol and hydroquinone. Ascorbate and a Vitamin E analogue are also oxidized very rapidly. N-Methylindole is oxidized by I atoms to its radical cation with a diffusion-controlled rate constant, 1.9 × 1010 L mol-1 s-1. Iodine atoms also oxidize sulfite and ferrocyanide ions rapidly but do not add to double bonds. The phenyl radicals, produced along with the I atoms, react with O2 to give phenylperoxyl radicals, which react with phenols much more slowly than I atoms. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 1197-1209 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear free-energy (LFE) correlations for gas phase O(3P) and OH addition and abstraction reactions with a number of organic compounds have been established using existing room-temperature rate constants evaluated from the literature. Addition reaction rate constant correlations with ionization potential and abstraction reaction rate constant correlations with bond dissociation energies are examined and compared to the LFE approach. Using multiple regression analysis, empirical linear equations are derived and used to predict rate constants for reactions of O(3P) and OH with a number of organic molecules. The use of LFE room-temperature rate predictions permits chemical modeling efforts to be extended to compounds where experimental determinations of rate coefficients are lacking and also serves as a useful tool in evaluation of experimental rate measurements.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 669-677 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The technique of laser photolysis of alkyl and perfluoroalkyl iodides at 266 nm followed by time-resolved detection of the 1.3-μm emission from I*(2P1/2) has been used to measure the rate constants for deactivation of I* by CH3I, C2H5I, CF3I, and CH4. The recommended values are (2.76± 0.22) × 10-13, (2.85 ± 0.40) × 10-13, (3.5 ± 0.5) × 10-17, and (7.52 ± 0.12) × 10-14, respectively, in units of cm3 molecule-1 S-1.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 1151-1164 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal decomposition of CF2HCl has been modeled using 2,269 thermally activated reactions and 63 chemically activated processes. Thermochemical properties for the species involved are calculated using statistical mechanics and group contribution theory, and reaction rate constants are determined using transition state theory. The theoretical predictions, obtained without fitting any parameter values, afree closely with available experimental data. Also, the reactions that control the distribution of reaction products are identified, and this, in turn, permits simplification of the reaction set. Sensitivity studies show that uncertainties in the calculations do not alter the predicted trends in behavior or the main reaction pathways. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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