Kinetic Study of the Oxidation of Catechol by Aqueous Copper(II)

The kinetics of the oxidation of catechol by aqueous copper(II) have been studied as a function of reactant concentrations at pH 6.4−7.2. To follow the reaction, a spectrophotometric method has been developed that circumvents the problem of precipitation of decomposition products of the initial o-qu...

Full description

Saved in:
Bibliographic Details
Published inInorganic chemistry Vol. 41; no. 12; pp. 3076 - 3083
Main Authors Kamau, P, Jordan, R. B
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 17.06.2002
Online AccessGet full text

Cover

Loading…
More Information
Summary:The kinetics of the oxidation of catechol by aqueous copper(II) have been studied as a function of reactant concentrations at pH 6.4−7.2. To follow the reaction, a spectrophotometric method has been developed that circumvents the problem of precipitation of decomposition products of the initial o-quinone oxidation product. The rate law shows that the reactive species is the monocatecholate complex of CuII, and that this species undergoes rate-limiting intramolecular electron transfer with k = 1.9 × 10-5 s-1 (22 ± 1 °C, μ = 0.125 M NaClO4). The results have allowed a reanalysis of previous work on the autoxidation in the aqueous CuII−catechol−dioxygen system, and comparisons to mechanisms of copper(II) oxidases.
Bibliography:istex:F4B425556F6321FADE154AA25542AF050DCBB906
ark:/67375/TPS-8TC683GW-G
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0020-1669
1520-510X
DOI:10.1021/ic010978c