Abstract
Diastereoisomeric chelate complexes of the type [FeL(N3)](L = a quadridentate Schiff base derived from 1,2-di-substituted ethylenediamine and salicylaldehyde) show differences in several aspects of their electrode behaviour, including the parameters for heterogeneous electron transfer, adsorption on the electrode, and the equilibrium constant of axial-ligand dissociation coupled with the electrochemical reduction.

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