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Kinetics and Mechanistic Study of the Ruthenium(III) Catalysed Oxidative Decarboxylation of L-Proline by Alkaline Heptavalent Manganese (Stopped flow technique)
Author(s) -
Ramesh S. Shettar,
Mallikarjuna I. Hiremath,
Sharanappa T. Nandibewoor
Publication year - 2004
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2005/369650
Subject(s) - chemistry , ionic strength , permanganate , kinetics , ruthenium , inorganic chemistry , catalysis , manganese , activation energy , alkali metal , stoichiometry , reaction mechanism , reaction rate constant , reaction rate , proline , photochemistry , aqueous solution , organic chemistry , amino acid , physics , quantum mechanics , biochemistry
The kinetics of ruthenium(III) catalysed oxidation of L-Proline by permanganate in alkaline medium at a constant ionic strength has been studied spectrophotometrically using a rapid kinetic accessory. The reaction between permanganate and L-Proline in alkaline medium exhibits 2:1 stoichiometry (KMnO4: L-Proline). The reaction shows first order dependence on [permanganate] and [ruthenium(III)] and apparent less than unit order dependence each in L-Proline and alkali concentrations. Reaction rate increases with increase in ionic strength and decrease in solvent polarity of the medium. Initial addition of reaction products did not affect the rate significantly. A mechanism involving the formation of a complex between catalyst and substrate has been proposed. The activation parameters were computed with respect to the slow step of the mechanism and discusse

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