摘要
A tritopic, Ni-substituted Keggin cluster, {SiW9Ni4}, assembles with rigid dicarboxylate linkers to give rise to a set of discrete, POM2nL3n-type structures (POM={SiW9Ni4}) with defined interior voids. The outcome of coordination-driven self-assemblies of these polyhedral cages—from fused dimers to trigonal prisms—was found to be sensitive to bend angles of the ditopic ligands, which vary from 122° to 180°. These polyoxotungstate-based metal–organic polyhedra, when coupled with [Ru(bpy)3]Cl2 as a photosensitizer and triethanolamine as the electron donor, serve as highly effective catalysts for CO2 reduction, with turnover numbers up to 328 and CO selectivity as high as 96.2 %. The inner cavities of such cage structures, if functionalized or of sufficient size to encapsulate targeted guest molecules, could present a new strategy towards functional materials for potential applications.
源语言 | 英语 |
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文章编号 | e202117637 |
期刊 | Angewandte Chemie - International Edition |
卷 | 61 |
期 | 19 |
DOI | |
出版状态 | 已出版 - 2 5月 2022 |