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首页> 外文期刊>Journal of Catalysis >Efficient heterogeneous catalytic systems for enantioselective hydrogenation of prochiral carbonyl compounds
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Efficient heterogeneous catalytic systems for enantioselective hydrogenation of prochiral carbonyl compounds

机译:用于前手性羰基化合物对映选择性氢化的高效多相催化体系

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A proficient heterogeneous catalyst system for stereoselective hydrogenation of carbonyl compounds was synthesized, involving anchoring of Ru-II-phosphine-diamine complexes on the inner surfaces of organo-functionalized mesoporous MCM-41 and MCM-48 materials. Powder XRD and TEM experiments reveal highly ordered hexagonal and cubic patterns of the organically modified MCM-41 and MCM-48 materials, respectively, even after incorporation of Ru complexes. Moreover, the integrity of the Ru complexes was retained after anchoring into the mesoporous hosts, which was supported from FTIR, P-31 CP MAS NMR, and XPS analyses. This new heterogeneous catalyst shows promising activity and selectivity in the enantioselective hydrogenation of prochiral ketones. The effects of reaction time, temperature, and hydrogen pressure on the catalytic activity and enantioselectivity were studied in detail. As high as 95-99% ee could be obtained using these solid catalysts under heterogeneous reaction conditions. The anchored solid catalysts can be recycled effectively and reused several times without any loss in activity and selectivity. (C) 2004 Elsevier Inc. All rights reserved.
机译:合成了一种用于羰基化合物立体选择性加氢的高效多相催化剂体系,该体系涉及将Ru-II-膦-二胺配合物锚固在有机功能化介孔MCM-41和MCM-48材料的内表面上。粉末XRD和TEM实验表明,即使掺入Ru络合物,有机改性的MCM-41和MCM-48材料也分别具有高度有序的六边形和立方图案。此外,在锚定到中孔宿主中后,Ru络合物的完整性得以保留,这得到了FTIR,P-31 CP MAS NMR和XPS分析的支持。这种新的非均相催化剂在前手性酮的对映选择性氢化中显示出有希望的活性和选择性。详细研究了反应时间,温度和氢气压力对催化活性和对映选择性的影响。使用这些固体催化剂在非均相反应条件下可获得高达95-99%ee。锚固的固体催化剂可以有效地再循环并重复使用几次,而不会损失活性和选择性。 (C)2004 Elsevier Inc.保留所有权利。

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