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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 29 (1980), S. 315-320 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. By the standing-jet method the authors have studied the kinetics of autoxidation of the ethylenediamine tetraacetate complex of Fe2+ in neutral and acid media. From the kinetic results they infer the formation of an intermediate oxygen complex which interacts either with H+ or with a second Fe2+ ion. 2. In the system Fe2+-EDTA-O2, in an acid medium O2 is reduced by a radical mechanism via intermediate formation of HO2; in a neutral medium, directly to H2O2. 3. The authors obtain quantitative estimates of the rate constants of formation and further reactions of the oxygenated complex in the absence of ligands and substrates.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 28 (1979), S. 2031-2036 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. Using the stopped-flow method in a noncorrodable apparatus made from glass and Teflon, the effect of ascorbic acid on the kinetics of the autoxidation of Cu+dipy2 has been studied. 2. The “partial charge-transfer” oxygen complex has been reacted with ascorbate anion, the oxidation of Cu+dipy2 being accompanied predominantly by a two-electron reduction of O2 without the formation of intermediate superoxide radicals. 3. The oxygen adduct reacts predominantly with the nonionized form of ascorbic acid. Oxidation of Cu+dipy2 as a result of this reaction is accompanied by reduction of O2 either to H2O2 or to HO2.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 28 (1979), S. 2024-2031 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. By the stopped flow method it has been shown that acetate has no effect on the kinetics of the autoxidation of the dipyridyl complex of copper (I) (Cu+dipy2). Ethylenediaminetetraacetate effectively reacts with the oxygen adduct dipy2Cu+O2, malonic acid reacts with both the adduct and with the partial charge-transfer complex dipy2CuO2 +. 2. The reaction of the dianion of malonic acid with the partial charge-transfer complex occurs by a mechanism of replacement of the coordinated 2,2′-dipyridyl and is accompanied by reduction of O2 to the Superoxide radical. 3. Reaction of polydentate ligands with the adduct also occurs by the mechanism of replacement of 2,2′-dipyridyl. When the adduct reacts with the monoanion of malonic acid, O2 is reduced to HO2 . and when it reacts with the dianion O2 is reduced to O2 .−. 4. The reaction rate constants for replacement of 2,2′-dipyridyl in the complexes dipy2Cu+O2 and dipy2CuO2 + have been determined, as well as the absolute values of the reaction rate constants of HO2 with Cu+dipy2 and Cu2+dipy2.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 28 (1979), S. 1377-1380 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions 1. The substrate in the Cu(I) dipyridyl complex-oxygen-methanol system interacts with the coordinated oxygen, which is itself activated by partial charge transfer from the copper atom. 2. Rate constants for the one-and two-electron oxidation of methanol by the coordinated oxygen have been determined.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 461-494 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Analysis is made of reported results on the kinetics and mechanism of ascorbic acid oxidation with oxygen in the presence of cupric ions. The diversities due to methodological reasons are cleared up. A kinetic study of the mechanism of Cu2+ anaerobic reaction with ascorbic acid (DH2) is carried out. The true kinetic regularities of catalytic ascorbic acid oxidation with oxygen are established at 2.7 ≤ pH 〈 4, 5 × 10-4 ≤ [DH2] ≤ 10-2M, 10-4 ≤ [Cu2+] ≤ 10-3M, and 10-4 ≤ [O2] ≤ 10-3M: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm W}_0 = {}_{K1}[{\rm Cu}^{{\rm 2} +}][{\rm DH}_2][{\rm O}_2]{}^{0.5}/[{\rm H}^ +] $$\end{document} wherek1 (25°C) = 0.13 ± 0.01 M-0.5·sec-1. The activation energy for this reaction is E1 = 22 ± 1 kcal/mol. It is found by means of adding Cu+ acceptors (acetonitrile and allyl alcohol) that the catalytic process is of a chain nature. The Cu+ ion generation at the interaction of the Cu2+ ion with ascorbic acid is the initiation step. The rate of the chain initiation at [Cu2+] ± 10-4M, [DH2] ± 10-2M, 2.5 〈 pH 〈 4, is \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm W}_{\rm i} = {}_{K{\rm i,1}}[{\rm Cu}^{{\rm 2} +}]^2 [{\rm DH}_2]/[{\rm H}^ +] $$\end{document} whereki,1 (25°C) = (1.8 ± 0.3)M-1·sec-1, Ei,1 = 31 ± 2 kcal/mol. The reaction of the Cu+ ion with O2 is involved in a chain propagation, so that the rate of catalytic ascorbic acid oxidation for the system Cu2+—DH2—O2 is \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm W}_{\rm 0} = {}_{k{\rm 1}}[{\rm Cu}^ +][{\rm O}_2] $$\end{document} wherek1 (25°C) = (5 ± 0.5) × 104 M-1·sec-1. The Cu+ ion and a species interacting with ascorbate are involved to quadratic chain termination. By means of photochemical and flow electron spin resonance methods we obtained data characteristic of the reactivities of ascorbic acid radicals and ruled out their importance for the catalytic chain process. A new type of chain mechanism of catalytic ascorbic acid oxidation with oxygen is proposed: .
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 983-1005 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of the interaction of Cu+-α,α-dipyridyl complex (Cu+L2) with O2 in both neutral and acid media was studied by the stopped-flow method. The dependence of the mechanism on the acidity of the medium was established. In an acid medium H+ participated in a direct O2 reduction to HO2 by interaction with an oxygen adduct L2Cu+O2 formed without displacement of ligand molecules. In a neutral medium the reaction rate was limited by inner sphere charge transfer from Cu+ to O2 to form an oxygen “charge transfer” complex L2CuO+2. The latter interacted either with the second ion Cu+L2 or with the free ligand, or else it dissociated, reversibly or irreversibly, to form a radical anion O-2. The bimolecular rate constants of the oxygen “adduct” and “charge transfer” complex formation appeared to be kbi = (1.0 ± 0.1) × 105 and (1.5 ± 0.2) × 104M-1ċsec-1, respectively. The effective termolecular rate constants of O2 reduction to HO2 in an acid medium (with contribution from H+) and to O-2 in a neutral medium (with contribution from α,α-dipyridyl) were kter = 2.7 × 108 and 107M-2ċsec-1. The rate constants of the elementary steps were estimated. The auto-oxidation mechanism of the aquoion and complexes of Cu+ is discussed in terms of the results obtained.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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