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首页> 外文期刊>ChemCatChem >Mesoporous Silica Nanosphere-Supported Chiral Ruthenium Catalysts: Synthesis, Characterization, and Asymmetric Hydrogenation Studies
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Mesoporous Silica Nanosphere-Supported Chiral Ruthenium Catalysts: Synthesis, Characterization, and Asymmetric Hydrogenation Studies

机译:介孔二氧化硅纳米球负载的手性钌催化剂:合成,表征和不对称加氢研究。

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摘要

Chiral RuCl2-diphosphine-diamine complexes with a pendant siloxy group were synthesized and characterized by NMR spectroscopy and mass spectrometry. The Ru complexes were grafted onto three different types of mesoporous silica nano-spheres (MSNs) through the siloxane linkage, and the resulting MSN-supported Ru catalysts were highly active for the asymmetric hydrogenation of aromatic ketones, to afford chiral secondary alcohols, and racemic arylaidehydes, to give chiral primary alcohols. Excellent activities and enantioselectivities were observed for these MSN-supported Ru catalysts owing to readily accessible and uniform catalytic sites within the large channels of MSNs (diameters of > 2 nm) and short diffusion lengths for the organic compounds as a result of small nano-particle sizes of less than 1 μm. This catalyst immobilization strategy with MSN supports should be amenable to the design of many highly active and enantioselective heterogeneous asymmetric catalysts.
机译:合成了具有侧基甲硅烷氧基的手性RuCl2-二膦二胺配合物,并通过NMR光谱和质谱表征。通过硅氧烷键将Ru络合物接枝到三种不同类型的介孔二氧化硅纳米球(MSNs)上,并且所得MSN负载的Ru催化剂对芳族酮的不对称氢化反应具有很高的活性,从而提供了手性仲醇和外消旋体芳基醛,以提供手性伯醇。这些MSN负载的Ru催化剂具有出色的活性和对映选择性,这是由于在MSNs大通道(直径> 2 nm)中易于接近且均一的催化位点,以及由于小纳米颗粒而使有机化合物的扩散长度短尺寸小于1μm。 MSN载体的这种催化剂固定化策略应适合许多高活性和对映选择性的多相不对称催化剂的设计。

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