Cohen Seth M, Zhang Zhenjie, Boissonnault Jake A
Department of Chemistry and Biochemistry, University of California, San Diego , La Jolla, California 92093, United States.
Inorg Chem. 2016 Aug 1;55(15):7281-90. doi: 10.1021/acs.inorgchem.6b00828. Epub 2016 May 27.
Metal-organic frameworks (MOFs) are being increasingly studied as scaffolds and supports for catalysis. The solid-state structures of MOFs, combined with their high porosity, suggest that MOFs may possess advantages shared by both heterogeneous and homogeneous catalysts, with few of the shortcomings of either. Herein, efforts to create single-site catalytic metal centers appended to the organic ligand struts of MOFs will be discussed. Reactions important for advanced energy applications, such as H2 production and CO2 reduction, will be highlighted. Examining how these active sites can be introduced, their performance, and their existing limitations should provide direction for design of the next generation of MOF-based catalysts for energy-relevant, small-molecule transformations. Finally, the introduction of second-sphere interactions (e.g., hydrogen bonding via squaramide groups) as a possible route to enhancing the activity of these metal centers is reported.
金属有机框架(MOF)作为催化的支架和载体正受到越来越多的研究。MOF的固态结构及其高孔隙率表明,MOF可能兼具多相催化剂和均相催化剂的优点,而几乎没有两者的缺点。本文将讨论在MOF的有机配体支柱上创建单中心催化金属中心的努力。将重点介绍对先进能源应用重要的反应,如氢气生产和二氧化碳还原。研究如何引入这些活性位点、它们的性能以及它们现有的局限性,应为设计用于与能源相关的小分子转化的下一代MOF基催化剂提供指导。最后,报告了引入第二配位层相互作用(例如通过方酰胺基团的氢键作用)作为增强这些金属中心活性的可能途径。