Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan.
Chem Asian J. 2012 Jun;7(6):1394-400. doi: 10.1002/asia.201101020. Epub 2012 Mar 1.
Herein, we report a [NiRu] biomimetic system for O(2)-tolerant [NiFe]hydrogenases and demonstrate that electron donation to the [NiRu] center can switch the system between the activation of H(2) and O(2) through simple ligand effects by using hexamethylbenzene and pentamethylcyclopentadienyl ligands, respectively. Furthermore, we present the synthesis and direct observations of a [NiRu]-peroxo species, which was formed by the oxygenation of a Ni-SIa model [NiRu] complex, that we propose as a biomimetic analogue of O(2)-bound species (OBS) of O(2)-tolerant [NiFe]hydrogenases. The [NiRu]-peroxo complex was fully characterized by X-ray analysis, X-ray photoelectron spectroscopy (XPS), mass spectrometry, and (1)H NMR spectroscopy. The OBS analogue was capable of oxidizing p-hydroquinone and sodium borohydride to turn back into the Ni-SIa model complex.
本文报道了一种[NiRu]仿生体系,可用于耐氧[NiFe]氢化酶,并通过分别使用六甲基苯和五甲基环戊二烯基配体对[NiRu]中心进行电子供体,证明了通过简单的配体效应,该体系可以在 H(2)和 O(2)的活化之间切换。此外,我们还提出了一种[NiRu]-过氧物种的合成和直接观察,该物种是由 Ni-SIa 模型[NiRu]配合物的氧化形成的,我们将其作为耐氧[NiFe]氢化酶中 O(2)结合物种 (OBS) 的仿生模拟物。通过 X 射线分析、X 射线光电子能谱 (XPS)、质谱和 (1)H NMR 光谱对 [NiRu]-过氧配合物进行了全面表征。OBS 类似物能够将对苯二酚和硼氢化钠氧化为 Ni-SIa 模型配合物。