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金属有机骨架中的钛(III)-氧簇支撑单原子 Co(II)-氢化物催化剂用于芳烃加氢。

Titanium(III)-Oxo Clusters in a Metal-Organic Framework Support Single-Site Co(II)-Hydride Catalysts for Arene Hydrogenation.

机构信息

Department of Chemistry, University of Chicago , 929 E. 57th Street, Chicago, Illinois 60637, United States.

State Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100050, China.

出版信息

J Am Chem Soc. 2018 Jan 10;140(1):433-440. doi: 10.1021/jacs.7b11241. Epub 2017 Dec 19.

Abstract

Titania (TiO) is widely used in the chemical industry as an efficacious catalyst support, benefiting from its unique strong metal-support interaction. Many proposals have been made to rationalize this effect at the macroscopic level, yet the underlying molecular mechanism is not understood due to the presence of multiple catalytic species on the TiO surface. This challenge can be addressed with metal-organic frameworks (MOFs) featuring well-defined metal oxo/hydroxo clusters for supporting single-site catalysts. Herein we report that the Ti(μ-O)(μ-OH) node of the Ti-BDC MOF (MIL-125) provides a single-site model of the classical TiO support to enable Co-hydride-catalyzed arene hydrogenation. The catalytic activity of the supported Co-hydride is strongly dependent on the reduction of the Ti-oxo cluster, definitively proving the pivotal role of Ti in the performance of the supported catalyst. This work thus provides a molecularly precise model of Ti-oxo clusters for understating the strong metal-support interaction of TiO-supported heterogeneous catalysts.

摘要

二氧化钛 (TiO) 在化学工业中被广泛用作有效的催化剂载体,得益于其独特的强金属-载体相互作用。许多建议已经提出,旨在从宏观层面上合理化这种效果,但由于 TiO 表面上存在多种催化物种,其潜在的分子机制尚不清楚。具有明确的金属氧/羟基金属簇的金属有机骨架 (MOF) 可以解决这一挑战,用于支持单原子催化剂。在此,我们报告说 Ti-BDC MOF (MIL-125) 的 Ti(μ-O)(μ-OH) 节点为经典 TiO 载体提供了单原子模型,从而实现了 Co-氢化物催化的芳烃加氢。负载 Co-氢化物的催化活性强烈依赖于 Ti-氧簇的还原,这明确证明了 Ti 在负载催化剂性能中的关键作用。因此,这项工作为理解 TiO 负载多相催化剂的强金属-载体相互作用提供了一个分子精确的 Ti-氧簇模型。

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