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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 7939-7941 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 4304-4306 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Transition metal chemistry 18 (1993), S. 218-220 
    ISSN: 1572-901X
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary The kinetics of the reaction of manganese(III) with oxalic acid (OA) has been studied in H2SO4 solutions. Under the experimental conditions of 6 × 10−3 〈 [OA]0 〈 0.4 mol dm−3 and [H2SO4]0 ⩾ 0.2 mol dm−3 the observed pseudo-first order rate constant k obs follows the expression $$k_{obs} = k_1 + k_2 K_2 \left[ {C_2 O_4^{2 - } } \right]/\left\{ {1 + K_2 \left[ {C_2 O_4^{2 - } } \right]} \right\}$$ where k 1, k 2 and K 2 have been estimated by a non-linear least-squares method. The kinetics of this component reaction of the BZ type oscillation system with oxalic acid was influenced by the addition of HSO f4 p− , SO f4 p2+ and ClO f4 p− ions. Oxalate complexes of manganese(III) decompose by a net process that can be generalized as 2MnIII + C2O f4 p2− → 2MnII + 2CO2.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Transition metal chemistry 23 (1998), S. 801-805 
    ISSN: 1572-901X
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The dependence of the rate constants for the oxidation of [Co(en)2amS]2+ (amS=–SCH2CH2NH2 2− by IO4− on solvent composition has been established for aqueous mixtures of MeOH, i-PrOH, t-BuOH, urea (U), ethylene carbonate (EC), acetonitrile (AN), dimethyl formamide (DMF) and acetone (Me2CO). Addition of aprotic cosolvents leads to marked decrease in the reaction rate in comparison to monohydroxylic alcohols. Alcohols inhibit the reaction rate in order MeOH 〈 i-PrOH 〈 t-BuOH. The change in solvation on going from the initial to the transition state are discussed in terms of the Gibbs transfer function, ΔGt0.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 26 (1994), S. 347-353 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Complex dynamical behavior has been observed in the oxidation of hydroxylamine by bromate in acidic sulfate medium. The reaction shows clock type kinetics in closed conditions and an aperiodic oscillations if gaseous products are removed from the system with a constant flow-rate. The reduction kinetics of bromate ions with excess hydroxylamine has been studied in the presence of allyl alcohol. The observed pseudo-first-order rate constant kobs has been found to follow the expression \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{{\rm obs}} = \frac{{kK_1 \left[{{\rm H}^ +} \right]\left[{{\rm hydroxylamine}} \right]}}{{\left({1 + {\rm K}_{\rm 1} \left[{{\rm H}^ +} \right]} \right){\rm K}_{\rm 2}}} $$\end{document} where [hydroxylamine] is total initial hydroxylamine concentration, K1 = 0.5 M-1, K2 = 106 M-1, and k = 2.57 × 103 M-1 s-1 at 298.15 K and I = 2.0 M.The rate constant for the bromine oxidation of hydroxylamine in sulfuric aqueous solution has been determined. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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