ELECTROCHEMICAL OXYGEN REDUCTION MEDIATED BY COPPER(I) AND IRON(II) COMPLEXES IN CHLORIDE MOIETY - A NEW ROUTE FOR TOLUENE OXIDATION

Citation
R. Tomat et al., ELECTROCHEMICAL OXYGEN REDUCTION MEDIATED BY COPPER(I) AND IRON(II) COMPLEXES IN CHLORIDE MOIETY - A NEW ROUTE FOR TOLUENE OXIDATION, Electrochimica acta, 39(16), 1994, pp. 2475-2479
Citations number
34
Categorie Soggetti
Electrochemistry
Journal title
ISSN journal
00134686
Volume
39
Issue
16
Year of publication
1994
Pages
2475 - 2479
Database
ISI
SICI code
0013-4686(1994)39:16<2475:EORMBC>2.0.ZU;2-R
Abstract
The potentiostatic reduction of Cu(II) in HCl solutions saturated by O -2 was investigated to determine the competition of redox reactions be tween Cu(I), O-2, and Cl-. Cu(I) reacts with O-2 to form OH radicals, which in turn oxidize Cl- to Cl radicals. When the radical scavenger t oluene is added to the electrolytic environment, benzaldehyde and benz ylchloride are obtained. In Fe(III)/Na4P2O7 solutions saturated by O-2 , OH radicals are produced by the reaction between electrogenerated re agents Fe(II) and H2O2. In the presence of toluene, cresols are the ma in products, largely prevailing over benzaldehyde. The parameters dete rmining the distribution of such products were also investigated.