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Design of Air and Moisture Stable Ruthenophane and Ruthenium(II)-p Complexes and Study of Their Applications in Catalysis

机译:空气和湿气稳定的卢斯烯烷和钌(II)-P复合物的设计及其在催化中的应用

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Herein, we report the synthesis and characterization of two ruthenophane (1) and ruthenium(II)-p (2) complexes, and the results of their catalytic applications under different conditions. These complexes exhibited excellent air and moisture stability due to the existence of effective cation-p interactions between the metal ion and the aromatic surface of the ligand. These complexes were tested and compared in the transfer hydrogenation of acetophenone in 2-propanol. The ruthenophane complex 1 exhibited highest efficiency in the catalytic transfer hydrogenation reaction when compared to the complex 2. The better efficiency of the complex 1 can be ascribed to the steric and cation-p interactions of the cyclophane ligands with the metal centre under reaction conditions. Using catalyst loading of ca. 2 mol%, the transfer hydrogenation of the aromatic ketones having different substituents was achieved. Notably, these complexes exhibited high selectivity for the aromatic ketones having electronegative substituents and showed highest efficiency of ca. 100% under moderate reaction conditions when compared to the literature known ruthenium catalysts.
机译:本文中,我们报告了两种正确的(1)和氟苯二(II)-p(2)复合物的合成和表征,以及在不同条件下其催化应用的结果。由于金属离子和配体的芳香族表面之间存在有效的阳离子-P相互作用,这些复合物表现出极好的空气和水分稳定性。对这些复合物进行了测试,并比较了2-丙醇中苯乙酮的转移氢化。与复合物2相比,正确的苯烷复合物1在催化转移氢反应中表现出最高的效率。在反应条件下,环烷配体与金属中心的空间和阳离子-P相互作用的较高效率可以归因于空间和阳离子-P相互作用。使用Ca的催化剂负载。 2 mol%,实现了具有不同取代基的芳族酮的转移氢化。值得注意的是,这些复合物对具有电负性取代基的芳族酮表现出很高的选择性,并且效率最高。与文献已知的芳族催化剂相比,在中度反应条件下有100%。

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