Author： Bagiyan G. A. Koroleva I. K. Soroka N. V. Ufimtsev A. V.
Publisher： MAIK Nauka/Interperiodica
ISSN： 0023-1584
Source： Kinetics and Catalysis, Vol.45, Iss.3, 2004-05, pp. : 372-380
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Abstract
The kinetics of the catalytic oxidation reactions of thiol compounds with molecular oxygen in aqueous solutions in the presence of copper ions was studied in relation to the structures of oxidized thiols and the pH of the solution. A modified procedure used for the determination of [O2] allowed us to obtain the kinetic characteristics of more than 30 thiols over a wide pH range. We found that weakly chelating thiols exhibited a first order of reaction with respect to [Cu+] and [O2] under conditions when the [(Cu+)(RS–)2] complex occurred. In the oxidation of strongly chelating thiols in an alkaline medium, the order of reaction with respect to [Cu+] was equal to 2, and the rate of reaction was independent of [O2]. We found that the introduction of small amounts of strongly chelating thiols into Cu+ solutions containing difficult-to-oxidize mercaptans resulted in a dramatic acceleration of mercaptan oxidation. We hypothesized that O2 was effectively bound to the [(Cu+)(RS–)2] complexes in an alkaline medium in the case of strongly chelating thiols, and this was not the case with the complexes of weakly chelating thiols.
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