Active-site models for iron hydrogenases: reduction chemistry of dinuclear iron complexes

Inorg Chem. 2006 Oct 2;45(20):8000-2. doi: 10.1021/ic0610381.

Abstract

Reduction of Fe2(mu-S2C3H6)(CO)6 (1) in tetrahydrofuran with 1 equiv of decamethylcobaltocene (Cp*2Co) affords a tetranuclear dianion 2. The IR spectra of samples of 2 in solution and in the solid state exhibit a band at 1736 cm(-1), suggestive of the presence of a bridging carbonyl (CO) ligand. X-ray crystallography confirms that the structure of 2 consists of two Fe2 units bridged by a propanedithiolate moiety formulated as [Fe2(mu-S2C3H6)(CO)5(SCH2CH2CH2-mu-S)Fe2(mu-CO)(CO)6](2-). One of the Fe2 units has a bridging CO ligand and six terminal CO ligands. The second subunit exhibits a bridging propanedithiolate moiety. One CO ligand has been replaced by a terminal thiolate ligand, replicating the basic architecture of Fe-only hydrogenases. The reduction reaction can be reversed by treatment of 2 with 2 equiv of [Cp2Fe][PF6], reforming complex 1 in near-quantitative yield. Complex 2 can also be oxidized by acids such as p-toluenesulfonic acid, regenerating complex 1 and forming H2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Crystallography, X-Ray
  • Furans / chemistry
  • Hydrogenase / chemistry*
  • Iron / chemistry*
  • Iron-Sulfur Proteins / chemistry*
  • Models, Molecular
  • Organometallic Compounds / chemistry*
  • Spectrophotometry, Infrared

Substances

  • Furans
  • Iron-Sulfur Proteins
  • Organometallic Compounds
  • tetrahydrofuran
  • Iron
  • iron hydrogenase
  • Hydrogenase