4.7 Article

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

Journal

DALTON TRANSACTIONS
Volume -, Issue 35, Pages 4747-4755

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b807555g

Keywords

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Funding

  1. Chemistry of Concerto Catalysis [17350027]
  2. Global COE Program [17655027]
  3. Science for Future Molecular Systems [18033041]
  4. Ministry of Education, Culture, Sports, Science and Technology, Japan [18065017 (Chemistry of Concerto Catalysis), and the Global COE Program, Science for Future Molecular Systems from the]

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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.

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