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Self-Supporting Metal-Organic Layers as Single-Site Solid Catalysts

机译:自支撑金属有机层作为单点固体催化剂

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摘要

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.
机译:金属有机层(MOL)代表了新兴的一类可调谐和可功能化的二维材料。在这项工作中,由[Hf6O4(OH)(4)(HCO2)(6)]二级结构单元(SBU)和苯-1,3,5-三苯甲酸酯(BTB)桥联构成的自支撑MOL的可扩展溶剂热合成报告了配体。 MOL结构直接通过TEM和AFM成像,并掺入4-(4-苯甲酸酯)-(2,2,2-叔吡啶)-5,5-二羧酸酯(TPY),然后与铁中心配位以提供高活性和可重复使用的单中心固体催化剂用于末端烯烃的氢化硅烷化。基于MOL的非均相催化剂不受所有已知的多孔固体催化剂(包括金属有机骨架)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,并为一类具有分子功能的新型二维配位材料打开了大门。

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