College of Chemistry and Chemical Engineering, iCHEM, PCOSS, Xiamen University, Xiamen, 361005, China.
Department of Chemistry, University of Chicago, Chicago, IL, 60637, USA.
Angew Chem Int Ed Engl. 2016 Apr 11;55(16):4962-6. doi: 10.1002/anie.201512054. Epub 2016 Mar 8.
Metal-organic layers (MOLs) represent an emerging class of tunable and functionalizable two-dimensional materials. In this work, the scalable solvothermal synthesis of self-supporting MOLs composed of [Hf6O4(OH)4(HCO2)6] secondary building units (SBUs) and benzene-1,3,5-tribenzoate (BTB) bridging ligands is reported. The MOL structures were directly imaged by TEM and AFM, and doped with 4'-(4-benzoate)-(2,2',2''-terpyridine)-5,5''-dicarboxylate (TPY) before being coordinated with iron centers to afford highly active and reusable single-site solid catalysts for the hydrosilylation of terminal olefins. MOL-based heterogeneous catalysts are free from the diffusional constraints placed on all known porous solid catalysts, including metal-organic frameworks. This work uncovers an entirely new strategy for designing single-site solid catalysts and opens the door to a new class of two-dimensional coordination materials with molecular functionalities.
金属-有机层(MOLs)代表了一类新兴的可调谐和功能化的二维材料。在这项工作中,报告了由[Hf6O4(OH)4(HCO2)6]次级构筑单元(SBUs)和苯-1,3,5-三苯甲酸(BTB)桥联配体组成的自支撑 MOL 的可扩展溶剂热合成。通过 TEM 和 AFM 直接对 MOL 结构进行成像,并在与铁中心配位之前掺杂 4'-(4-苯甲酸)-(2,2',2''-三联吡啶)-5,5''-二羧酸酯(TPY),以提供用于末端烯烃氢硅烷化的高活性和可重复使用的单中心固体催化剂。基于 MOL 的多相催化剂不受所有已知多孔固体催化剂(包括金属有机骨架)所施加的扩散限制。这项工作揭示了设计单中心固体催化剂的全新策略,并为具有分子功能的新型二维配位材料开辟了道路。