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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 225-230 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the oxidation of formate, oxalate, and malonate by |NiIII(L1)|2+ (where HL1 = 15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-en-2-one oxime) were carried out over the regions pH 3.0-5.75, 2.80-5.50, and 2.50-7.58, respectively, at constant ionic strength and temperature 40°C. All the reactions are overall second-order with first-order on both the oxidant and reductant. A general rate law is given as - d/dt|NiIII(L1)2+| = kobs|NiIII(L1)2+| = (kd + nks |R|)|NiIII(L1)2+|, where kd is the auto-decomposition rate constant of the complex, ks is the electron transfer rate constant, n is the stoichiometric factor, and R is either formate, oxalate, or malonate. The reactivity of all the reacting species of the reductants in solution were evaluated choosing suitable pH regions. The reactivity orders are: kHCOOH 〉 kHCOO-; kH2ox 〉 kHox- 〉 kox2-, and kH2mal 〉 kHmal- 〈 kmal2- for the oxidation of formate, oxalate, and malonate, respectively, and these trends were explained considering the effect of hydrogen bonded adduct formation and thermodynamic potential. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 225-230, 1997.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 649-656 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the oxidation of thiosulfate ion by [Mn(Y)]- (H4Y = trans-cyclohezane-1,2-dimine-N,N,N′,N′-tetraacetic acid) and [Ni(L1)]2+ (HL1 = 15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-en-2-one oxime) have been investigated at 20.0, 30.0, and 40.0°C in aqueous solution and found to follow the general rate law -d/dt [complex] = kox[S2O32-] [complex]. The large negative entropy (ΔS
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 81-94 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of oxidation of cyclohexanone(chxn), 2-butanone(but), and 1,3-dihydroxy-2-propanone (dhp) have been investigated in aqueous acidic media. A first-order dependence in complex is obtained at high acid and low oxidant concentration for these ketones. However, a zero-order rate prevails at high oxidant and low acid concentration, and this rate has been shown to be the acid catalyzed enolization rate of the ketone. A general rate expression has been derived to explain these behaviors and plausible mechanism has been offered by assuming the enol as the reactive species.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the reactions of manganese(III) complexes of trans-cyclohexane-1,2-diamine-NNN′N′-tetraacetic acid (H4cydta) and 2,2′-bipyridyl (bpy) have been investigated in the acid ranges [H+] = 1.00 ×10-5 - 3.16 × 10-3 M and [H+] = 0.10 - 1.00 M, respectively, at different temperatures and at a constant ionic strength. Both the molecular and mono-anionic forms of ascorbic acid have been found to be reactive in the experimental acid ranges. The monoanionic species has been found to be more reactive than the molecular form. Attempts have been made to correlate the kinetic results in terms of the Marcus relationship for outer-sphere electron transfer reaction. Differences between the calculated rates (k0.8) and experimental rates (k) by approximately four and seven orders of magnitude (k0.8≪ k) suggest an innersphere pathway for the reaction of Mn(cydta)(H2O)-. Inner-sphere reaction is also believed to be operative for the other reaction. The activation parameters have been evaluated and compared with other reported systems.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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