Electron transfer between bis(pyridine) meso-tetraphenylporphyrinato iron(II) and ruthenium(III) and the hexacyanof errate couple at the 1,2-dichlor

Abstract

Oxidation and reduction of iron and ruthenium metalloporphyrin complexes with pyridine in 1,2-dichloroethane (1,2-DCE) have been investigated. Redox potential shifts are observed for the two compounds on complexation. Electron transfer reactions between these two complexes in the organic phase and the aqueous ferri-ferrocyanide couple have been studied at the 1,2-DCE/water interface, for which a quasi-reversible one-electron transfer was found, whereas reversible behaviour was observed at metallic electrodes. Possible explanations for this difference are discussed in terms of orientation and ligand effects.