Mechanism of H2 production by the [FeFe]H subcluster of di-iron hydrogenases: Implications for abiotic catalysts

Carlo Sbraccia, Federico Zipoli, Roberto Car, Morrel H. Cohen, G. Charles Dismukes, Annabella Selloni

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

To explore the possibility that the active center of the di-iron hydrogenases, the [FeFe]H subcluster, can serve by itself as an efficient hydrogen-producing catalyst, we perform comprehensive calculations of the catalytic properties of the subcluster in vacuo using first principles density functional theory. For completeness, we examine all nine possible geometrical isomers of the Fe(II)Fe(I) active-ready state and report in detail on the relevant ones that lead to the production of H2. These calculations, carried out at the generalized gradient approximation level, indicate that the most efficient catalytic site in the isolated [FeFe] H subcluster is the Fed center distal (d) to the [4Fe-4S]H cluster; the other iron center site, the proximal Fe p, also considered in this study, has much higher energy barriers. The pathways with the most favorable kinetics (lowest energy barrier to reaction) proceed along configurations with a CO ligand in a bridging position. The most favorable of these CO-bridging pathways start from isomers where the distal CN- ligand is in up position, the vacancy V in down position, and the remaining distal CO is either cis or trans with respect to the proximal CO. These isomers, not observed in the available enzyme X-ray structures, are only marginally less stable than the most stable nonbridging Fed-CO-terminal isomer. Our calculations indicate that this CO-bridging CN-up isomer has a small barrier to production of H2 that is compatible with the observed rate for the enzyme. These results suggest that catalysis of H2 production could proceed on this stereochemically modified [FeFe]H subcluster alone, thus offering a promising target for functional bioinspired catalyst design.

Original languageEnglish
Pages (from-to)13381-13390
Number of pages10
JournalJournal of Physical Chemistry B
Volume112
Issue number42
DOIs
Publication statusPublished - Oct 23 2008

    Fingerprint

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

Cite this