pH-Dependent isotope exchange and hydrogenation catalysed by water-soluble NiRu complexes as functional models for [NiFe]hydrogenases

Dalton Trans. 2008 Sep 21:(35):4747-55. doi: 10.1039/b807555g. Epub 2008 Jul 30.

Abstract

The pH-dependent hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes and hydrogenation of the carbonyl compounds have been investigated with water-soluble bis(mu-thiolate)(mu-hydride)NiRu complexes, Ni(II)(mu-SR)(2)(mu-H)Ru(II) {(mu-SR)(2) = N,N'-dimethyl-N,N'-bis(2-mercaptoethyl)-1,3-propanediamine}, as functional models for [NiFe]hydrogenases. In acidic media (at pH 4-6), the mu-H ligand of the Ni(II)(mu-SR)(2)(mu-H)Ru(II) complexes has H(+) properties, and the complexes catalyse the hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes. A mechanism of the hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes through a low-valent Ni(I)(mu-SR)(2)Ru(I) complex is proposed. In contrast, in neutral-basic media (at pH 7-10), the mu-H ligand of the Ni(II)(mu-SR)(2)(mu-H)Ru(II) complexes acts as H(-), and the complexes catalyse the hydrogenation of carbonyl compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Hydrogen-Ion Concentration
  • Hydrogenase / chemistry*
  • Hydrogenase / metabolism*
  • Hydrogenation
  • Isotopes / chemistry
  • Models, Biological
  • Models, Chemical
  • Nickel / chemistry*
  • Organometallic Compounds / chemistry*
  • Protons
  • Ruthenium / chemistry*
  • Solubility
  • Water / chemistry*

Substances

  • Isotopes
  • Organometallic Compounds
  • Protons
  • Water
  • Nickel
  • Ruthenium
  • nickel-iron hydrogenase
  • Hydrogenase