J. Phys. IV France
Volume 04, Numéro C1, Janvier 1994
Récents Développements en Electrochimie Fondamentale et Appliquée
Page(s) C1-147 - C1-156
Récents Développements en Electrochimie Fondamentale et Appliquée

J. Phys. IV France 04 (1994) C1-147-C1-156

DOI: 10.1051/jp4:1994110

Chemins réactionnels en électrochimie organique : adsorption et protonation


Laboratoire de Synthèse et d'Electrosynthèse Organométalliques, URA 1685 du CNRS, Faculté des Sciences Gabriel, 6 bd Gabriel, 21000 Dijon, France

The electrochemical reduction or oxidation of organic compounds in aqueous medium is characterized by two particular features. a) Practically all the organic substances are adsorbable, to a lesser or to a larger extent. b) Fast protonation of the intermediates leads to apparent global n-electron reactions. The effects of the adsorption of the redox species are first analyzed. It is shown that for weak or intermediate adsorption (mobile film) the reaction appears as heterogeneous, with an apparent constant khappad, whose order of magnitude is about 104 to 106 times larger than the "normal" heterogeneous rate constant. This is because reduction or oxidation takes place via a surface reaction, whose rate constant ks is very large (of the order of 109s-1). Both khappad and ks are too large to be determined by existing electrochemical methods. The theory of square (cubic, bicubic, etc...) schemes with protonations at equilibrium shows that any of these reactions is equivalent to simple electrochemical reactions, whose apparent constants are much decreased, in comparison with the elementary rate constants. Application of this theory enabled us to determine ks and khappad for different compounds in the whole pH range ; several examples (4-nitropyridine and its N-oxide, ...) are presented. Our study confirms the order of magnitude indicated above for ks and khappad, and allows the detailed mechanism (sequence of addition of electron and protons) to be determined.

© EDP Sciences 1994