Abstract
Cubic metal-covalent-supramolecular organic framework (MCSOF-1) hybrid has been created from the reaction of two molecular components and subsequent co-assembly with cucurbit[8]uril (CB[8]) in water. In the presence of CB[8], [Ru(bpy)3]2+ -based acylhydrazine 1·2Cl reacted with aldehyde 2·Cl to quantitatively yield six-armed precursor 3·8Cl through the generation of MCSOF-1. MCSOF-1 combines the structural features of metal-, covalent- and supramolecular organic frameworks. Its periodicity in water and in the solid state was confirmed by synchrotron X-ray scattering and diffraction experiments. MCSOF-1 could enrich discrete anionic polyoxometalates (POMs), maintain periodicity in acidic medium, and remarkably facilitate visible light-induced electron transfer from its [Ru(bpy)3]2+ units to enriched POMs, leading to enhanced catalysis of the POMs for the reduction of proton to H2 in both aqueous (homogeneous) and organic (heterogeneous) media.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (21529201, 21432004, 91527301), the Molecular Foundry, Lawrence Berkeley National Laboratory, and the Office of Science, Office of Basic Energy Sciences, Scientific User Facilities Division, of the U.S. Department of Energy (DE-AC02- 05CH11231). We thank the Shanghai Synchrotron Radiation Facility for providing BL16B1 and BL14B1 beamlines for collecting the synchrotron X-ray scattering and diffraction data, and the SIBYLS Beamline 12.3.1 of the Advanced Light Source, Lawrence Berkeley National Laboratory, for collecting solutionphase synchrotron small-angle X-ray scattering data.
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A stable metal-covalent-supramolecular organic framework hy-brid: enrichment of catalysts for visible light-induced hydrogen production
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Li, XF., Yu, SB., Yang, B. et al. A stable metal-covalent-supramolecular organic framework hybrid: enrichment of catalysts for visible light-induced hydrogen production. Sci. China Chem. 61, 830–835 (2018). https://doi.org/10.1007/s11426-018-9234-2
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DOI: https://doi.org/10.1007/s11426-018-9234-2