Issue 21, 2003

Electrocatalysis of hydrogen production by active site analogues of the iron hydrogenase enzyme: structure/function relationships

Abstract

A series of binuclear FeIFeI complexes, (μ-SEt)2[Fe(CO)2L]2 (L = CO (1), PMe3 (1-P)), (μ-SRS)[Fe(CO)2L]2 (R = CH2CH2 (μ-edt): L = CO (2), PMe3 (2-P); R = CH2CH2CH2(μ-pdt): L = CO (3), PMe3 (3-P); and R = o-CH2C6H4CH2 (μ-o-xyldt): L = CO (4), PMe3 (4-P)), that serve as structural models for the active site of Fe-hydrogenase are shown to be electrocatalysts for H2 production in the presence of acetic acid in acetonitrile. The redox levels for H2 production were established by spectroelectrochemistry to be Fe0Fe0 for the all-CO complexes and FeIFe0 for the PMe3-substituted derivatives. As electrocatalysts, the PMe3 derivatives are more stable and more sensitive to acid concentration than the all-CO complexes. The electrocatalysis is initiated by electrochemical reduction of these diiron complexes, which subsequently, under weak acid conditions, undergo protonation of the reduced iron center to produce H2. An (η2-H2)FeII–Fe0/I intermediate is suggested and probable electrochemical mechanisms are discussed.

Graphical abstract: Electrocatalysis of hydrogen production by active site analogues of the iron hydrogenase enzyme: structure/function relationships

Supplementary files

Article information

Article type
Paper
Submitted
17 апр 2003
Accepted
30 май 2003
First published
22 сеп 2003

Dalton Trans., 2003, 4158-4163

Electrocatalysis of hydrogen production by active site analogues of the iron hydrogenase enzyme: structure/function relationships

D. Chong, I. P. Georgakaki, R. Mejia-Rodriguez, J. Sanabria-Chinchilla, M. P. Soriaga and M. Y. Darensbourg, Dalton Trans., 2003, 4158 DOI: 10.1039/B304283A

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