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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 23-24 
    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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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 45-58 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constant for tert-butyl radical recombination has been measured near 700°K by the very-low-pressure pyrolysis (VLPP) technique and was found to be 108.8±0.3 M-1·sec-1 with neglibible temperature dependence. The thermochemical parameters for tert—butyl radicals were varied within reasonable limits to bring into agreement the data for the decomposition of 2,2,3,3-tetramethyl butane and the recombination of tert-butyl radicals. The revised thermochemistry also makes the gas-phase results and liquid-phase results compatible.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 641-649 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Diels-Alder addition of acrolein to cyclohexa-1,3-diene has been studied between 486 and 571°K at pressures ranging from 55 to 240 torr. The products are endo- and exo-5-formylbicyclo[2.2.2]oct-2-ene (endo- and exo-FBO), and their formations are second order. The rate constants (in l./mole · sec) are given by \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} {\rm}k_{{\rm endo}} = -(19,470 \pm 50)/4.576T + (5.65 \pm 0.02)$$\end{document}\documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} {\rm}k_{{\rm exo}} = - (20,630 \pm 50)/4.576T + (5.51 \pm 0.02)$$\end{document}The retro-Diels-Alder pyrolysis of endo-FBO has also been studied. In the ranges of 565-638°K and 6-38 torr, the reaction is first order, and its rate constant (in sec-1) is given by \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} {\rm}k_{{\rm p}} = - (46,390 \pm 110)/4.576T + (12.98 \pm 0.04)$$\end{document}The reaction mechanism is discussed. The heat of formation and the entropy of endo-FBO are estimated.
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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.
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  • 5
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photochemistry of azoethane and hexafluoroazomethane at 366 nm has been reinvestigated up to 1 atm pressure, and over a range of temperature from 27 to 150°C. The Stern-Volmer type quenching plots primarily demonstrate the decomposition of a single electronic and vibrationally excited state for azoethane, but competitive photodissociation from two different electronic and vibrationally excited states, which was previously postulated for hexafluoroazomethane and azoisopropane, is confirmed for hexafluoroazomethane. It is concluded, however, that two different electronic and vibrationally excited photodissociating states are present in azoethane photolysis, but that one of them is difficult to detect, at least by the present approachPhotosensitization with biacetyl at 436 nm also causes the dissociation of azoethane, and this is probably from the vibrationally equilibrated first triplet state. The energy barrier for this process was found to be 5.0 kcal/mol.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 825-857 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New experimental data have been obtained for H + C2H2, D + C2H2, H + C2D2, and D + C2D2 at room temperature. Two previously described apparatus were used in order to measure the pressure dependence of the reactions. The absolute rate constants are compared to results from other laboratories. The present results and those of Payne and Stief are used to obtain the high-pressure limiting rate constant at room temperature. When the activation energy from the work of Payne and Stief is considered, it is shown that the A factor for H + C2H2 is too low by a factor of ∼20. If a transmission coefficient is introduced which is constant for all isotopic variations, the pressure dependence can be explained in terms of the randomly energized radicals. RRKM theory is then invoked to explain the observed statistical nonequilibrium kinetic isotope effects.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 411-423 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Co(NH3)5OH23+ ion reacts with malonate to form Co(NH3)5O2CCH2CO2H2+ or Co(NH3)5O2CCH2CO2+, depending on the pH of the reaction solution. The kinetics of this anation reaction have been studied as a function of [H+] for the acidity range 1.5 ≤ pH ≤ 6.0 in the temperature range of 60 to 80°C, the [total malonate] ≤ 0.5 M, and the ionic strength 1.0M. The anation by malonic acid follows second-order kinetics, the rate constant being 8.0 × 10-5 M-1·sec-1 at 70°C, and the anations by bimalonate (Q1, k1) and malonate ion (Q2, k2) are consistent with an Id mechanism. Typical values at 70°C for the ion pair formation constants are Q1 = 1.3, Q2 = 5.4M-1; and for the interchange rate constants k1 = 5.3 × 10-4; k2 = 7.3 × 10-4 sec-1. The activation parameters for the various rate constants are reported and the results discussed with reference to previously reported data for similar systems.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 277-283 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrogen bromide is known to inhibit the bromination of aromatic substrates (ArH), either by fixing up bromine as HBr3 or ArH as ArH · HBr. However, there is catalysis by HBr in the bromination of mesitylene in acetic acid. The bromination of o-xylene in acetic acid in the dark is found to be autocatalytic, and the reaction is overall third order, first order in o-xylene with the orders in Br2 and HBr depending on the concentrations. A composite rate expression involving Br2 and HBr as electrophiles has been proposed and verified using iodine bromide as a catalyst where the orders are one in each of the reactants, irrespective of the concentrations used.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 651-671 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Atomic absorption and fluorescence spectrophotometry have been routinely used in kinetic investigations as probes of relative, rather than absolute, atom concentration. The calibration of a Lyman-α photometer for measurement of absolute hydrogen atom concentrations at levels [H] ι ≤ 1.8 × 1014 atoms/cm2 and total pressure of 1.5 torr He is described. The photometer is characterized in terms of a two-level emission source and an absorption region in which only Doppler broadening of the transition is considered. The modifications due to pressure broadening by high pressures (500 ≤ P ≤ 1500 torr) in the absorption region are discussed in detail. Application of the technique is reported for the recombination of hydrogen atoms in the presence of six nonreactive heat bath gases. Experiments were performed in a static reaction cell at pressures of 500-1500 torr of heat bath gas, and hydrogen atoms were produced by Hg (3P1) photosensitization of H2. The technique is critically evaluated and the mechanistic implications of the hydrogen atom recombination results are examined. The measured room temperature recombination rate constants in H2, He, Ne, Ar, Kr, and N2 are 8.5 ± 1.2, 6.9 ± 1.5, 5.9 ± 1.5, 8.0 ± 0.8, 10.2 ± 0.9, and 9.6 ± 1.4, respectively, where the units are 1033 cm6/molec2 · sec.
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