Kure Bunsho, Matsumoto Takahiro, Ichikawa Koji, Fukuzumi Shunichi, Higuchi Yoshiki, Yagi Tatsuhiko, Ogo Seiji
Center for Future Chemistry, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan.
Dalton Trans. 2008 Sep 21(35):4747-55. doi: 10.1039/b807555g. Epub 2008 Jul 30.
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.
已用水溶性双(μ-硫醇盐)(μ-氢化物)镍钌配合物Ni(II)(μ-SR)₂(μ-H)Ru(II) { (μ-SR)₂ = N,N'-二甲基-N,N'-双(2-巯基乙基)-1,3-丙二胺}作为[NiFe]氢化酶的功能模型,研究了气态同位素与介质同位素之间的pH依赖性氢同位素交换反应以及羰基化合物的氢化反应。在酸性介质(pH 4 - 6)中,Ni(II)(μ-SR)₂(μ-H)Ru(II)配合物的μ-H配体具有H⁺性质,且该配合物催化气态同位素与介质同位素之间的氢同位素交换反应。提出了通过低价Ni(I)(μ-SR)₂Ru(I)配合物进行气态同位素与介质同位素之间氢同位素交换反应的机理。相反,在中性 - 碱性介质(pH 7 - 10)中,Ni(II)(μ-SR)₂(μ-H)Ru(II)配合物的μ-H配体充当H⁻,且该配合物催化羰基化合物的氢化反应。