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Construction of Highly Active Ruthenium(II) NNN Complex Catalysts Bearing a Pyridyl-Supported Pyrazolyl-Imidazolyl Ligand for Transfer Hydrogenation of Ketones

机译:带有吡啶基负载的吡唑基-咪唑基配体的高活性钌(II)NNN络合物催化剂的构建,用于酮的加氢

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摘要

A family of hemilabile ruthenium(II) NNN complexes bearing a unsymmetrical 2-(benzoimidazol-2-yl)-6-(pyrazol-l-yl)pyridine ligand has been synthesized and exhibited good to excellent catalytic activity in transfer hydrogenation of ketones in refluxing 2-propanol, reaching final TOFs up to 7.2 x 10(5) h(-1) with 0.05 mol % loading. The gamma-NH effect of the benzoimidazol-2-yl moiety in the ligand and coordination modes of the metal center in a Ru(II) NNN complex has great influence on the catalytic activity of the complex catalyst in transfer hydrogenation of ketones. It has been demonstrated that one of the structural prerequisites for an active Ru(II) complex catalyst is the coordinatively unsaturated environment around the metal center in the complex or the precatalyst, and the catalytic activity of a complex catalyst can be enhanced by making its metal center cationic. This paper presents a methodology to construct new types of efficient Ru(II) complex catalysts for transfer hydrogenation of ketones.
机译:合成了一个带有不对称的2-(苯并咪唑-2-基)-6-(吡唑-1-基)吡啶配体的半不稳定钌(II)NNN配合物,在酮的氢化中表现出良好的催化活性。回流2-丙醇,以0.05 mol%的负载量达到7.2 x 10(5)h(-1)的最终TOF。 Ru(II)NNN配合物中配体中苯并咪唑-2-基部分的γ-NH效应和金属中心的配位模式对配合物催化剂在酮转移加氢中的催化活性有很大影响。已经证明,活性Ru(II)配合物催化剂的结构前提之一是配合物或预催化剂中金属中心周围的配位不饱和环境,并且可以通过使其金属来增强配合物催化剂的催化活性。中心阳离子。本文提出了一种方法来构造新型的高效Ru(II)络合物催化剂,用于酮的氢化转移。

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