含三齿席夫碱配体NOO供体的Ru(II)配合物的合成、表征、晶体结构和酮转移加氢催化活性

Premkumar Muniyappan , Vijayan Paranthaman , Venkatachalam Galmari
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引用次数: 0

摘要

一系列新的钳型钌(II)席夫碱配合物,即[Ru(CO)(PPh3)2(L1-6)](1-6)(其中,L1-6​=​三齿配体的NOO-供体)是由钌前体如含有三齿希夫碱配体(H2L1-H2L6)的[RuHCl(CO)(PPh3)3]合成的。通过元素分析和各种表征,如FT-IR、UV-Vis和NMR(1H和31P)光谱研究,对这些钌配合物进行了分析。配合物5([Ru(CO)(PPh3)2L5])的晶体结构通过单晶X射线晶体学测定,揭示了配合物的钳型配位模式。此外,配合物1-6已被用于在i-PrOH/KOH存在下将芳香酮转移氢化为仲醇。配合物的催化效率表明,酮与醇的转移加氢反应具有中高转化率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ru(II) complexes containing NOO donors of tridentate Schiff base ligands: Synthesis, characterization, crystal structure and catalytic activity in transfer hydrogenation of ketones

Ru(II) complexes containing NOO donors of tridentate Schiff base ligands: Synthesis, characterization, crystal structure and catalytic activity in transfer hydrogenation of ketones

A new series of pincer type ruthenium(II) Schiff base complexes namely [Ru(CO)(PPh3)2(L1‒6)] (1–6) (where, L1‒6 ​= ​NOO ‒ donors of tri-dentate ligands) have been synthesized from ruthenium precursor such as [RuHCl(CO)(PPh3)3] containing tri-dentate Schiff bases ligands (H2L1‒H2L6). These ruthenium complexes were analyzed by elemental analysis and diverse characterizations such as FT‒IR, UV–Vis and NMR (1H and 31P) spectroscopy studies. The crystal structure of one of the complexes 5 ([Ru(CO)(PPh3)2L5]) was determined by single crystal X‒ray crystallography that revealed pincer type of coordination mode of complexes. Furthermore, complexes 16 have been utilized for transfer hydrogenation of aromatic ketones to secondary alcohols in the presence of i‒PrOH/KOH. The catalytic efficiency of complexes showed an efficient for transfer hydrogenation of ketones with alcohol as moderate to high conversions.

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