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  • Articles  (4)
  • Physical Chemistry  (4)
  • 1970-1974  (4)
  • Chemistry and Pharmacology  (4)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • Articles  (4)
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  • Chemistry and Pharmacology  (4)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 487-493 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Shepp's rotating sector theory for determining radical recombination rate constants, kb, has been modified to take account of radical production by a concurrent thermal reaction. A theoretical sector curve expression has been derived which gives the average radical concentration under intermittent illumination as a function of α, the ratio of first-to second-order radical removal rates, n, the ratio of thermal initiation to photoinitiation, and β, the ratio of the flash time to the half time of second-order radical removal. Analysis of the sector curves generated by the modified theory shows that n has a greater effect on kb than α and that the rotating sector method should be applied only to those photochemical systems in which termination by first-order processes is less than 34% (α = 0.52) and thermal initiation is less than 2% (n = 0.02).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 323-336 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The substitution of N-alkyl substituted ethylenediamines for chloride ions in the rapidly equilibrating system \documentclass{article}\pagestyle{empty}\begin{document}$${\rm PdCl}_{\rm 4} ^{{\rm 2 - }} {\rm + H}_{\rm 2} {\rm O}\rightleftharpoons{\rm PdCl}_{\rm 3} ({\rm H}_2 {\rm O)}^{\rm - } + {\rm Cl}^{\rm - }$$\end{document} has been investigated in aqueous acid medium. The kinetic data can be accommodated by the general rate law \documentclass{article}\pagestyle{empty}\begin{document}$$k_{{\rm obs}} = \left\{ {\frac{k}{{\left[{{\rm H}^{\rm + }} \right]}} + \frac{{k'}}{{\left[{{\rm H}^{\rm + } } \right]\left[{{\rm Cl}^{\rm - } } \right]}}} \right\}\left[{{\rm N}_{\rm n} {\rm N}_{\rm m} {\rm en}} \right]_{{\rm total}}$$\end{document} where n = 0, 1, or 2 and m = 0, 1, or 2, depending on whether none, one, or two methyl groups are attached to the two nitrogen atoms of ethylenediamine. Reaction with the most heavily substituted ethylenediamine, namely, N2N2en discloses a change of the mentioned rate law to \documentclass{article}\pagestyle{empty}\begin{document}$$k_{{\rm obs}} = \left\{ {\frac{{k''}}{{\left[{{\rm H}^{\rm + } } \right]}} + \frac{{k'''\left[{{\rm Cl}^{\rm - } } \right]}}{{\left[{{\rm H}^{\rm + } } \right]}}} \right\}\left[{{\rm N}_{\rm 2} {\rm N}_{\rm 2} {\rm en}} \right]_{{\rm total}}$$\end{document} on going from a lower to a higher chloride ion concentration range. This change in the mathematical form of the rate law can be explained in terms of an ion-pair association of N2N2enH+ and free chloride ions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 309-321 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes PdCl42-, PdCl3(H2O)-, and PdCl3(Ac)2-, in rapid equilibrium with each other under the adopted experimental conditions, react with ethylenediamine according to the experimental rate law \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{{\rm obs}} = \left\{ {\frac{k}{{\left[{{\rm H}^{\rm + } } \right]}} + \frac{{k'}}{{\left[{{\rm H}^{\rm + } } \right]\left[{{\rm Cl}^{\rm - } } \right]}} + \frac{{k''\left[{{\rm Ac}^{\rm - } } \right]}}{{\left[{{\rm H}^{\rm + } } \right]\left[{{\rm Cl}^{\rm - } } \right]}}} \right\}\left[{{\rm en}} \right]_{{\rm total}}$$\end{document} A reaction scheme is proposed involving the reaction of enH+ with each of the above species, and the specific rate constants are computed. The activation parameters are given.
    Additional Material: 5 Ill.
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  • 4
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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