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Kinetics and mechanism of chromate reduction with hydrogen peroxide in base.

作者信息

Vander Griend Douglas A, Golden Joshua S, Arrington Charles A

机构信息

Department of Chemistry, Furman University, 3300 Poinsett Highway, Greenville, South Carolina 29613-1120, USA.

出版信息

Inorg Chem. 2002 Dec 30;41(26):7042-8. doi: 10.1021/ic0257975.

Abstract

Cr(VI)O(4)(-) is reduced to Cr(V)(O(2))(4)(-) by hydrogen peroxide in strongly basic media where the acid dissociation of H(2)O(2) (pK(a) = 11.65) is appreciable. The reaction is first order in chromium(VI) and inhibited by hydroxide. The hydrogen peroxide dependence is defined by the form of the effective pseudo-first-order rate constant: k(eff) = H(2)O(2)/(K(1) + K(2)[H(2)O(2)] + K(3)[HO(2)(-)]) with K(1) = 175(43) s x M(3), K(2) = 403(18) s x M(2), and K(3) = 1422(34) s x M(2). Hydrogen peroxide anion initially attacks chromate, and subsequent equilibrium steps that exchange oxo groups for three peroxo groups precede a rate-determining, one-electron, intramolecular reduction step.

摘要

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