期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 141, 期 40, 页码 15767-15772出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b08956
关键词
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资金
- MRSEC Shared User Facilities at the University of Chicago [NSF DMR-1420709]
- Materials Research Collaborative Access Team (MRCAT)
- U.S. DOE [DE-AC02-06CH11357]
Metal-organic layers (MOLs) have recently emerged as a novel class of molecular two-dimensional (2D) materials with significant potential for catalytic applications. Herein we report the design of a new multifunctional MOL, Hf-12-Ir-Ni, by laterally linking Hf(12)secondary building units (SBUs) with photosensitizing Ir(DBB)[dF(CF3)ppy](2)(+) [DBB-Ir-F, DBB = 4,4'-di(4-benzoato)-2,2'-bipyridine; dF(CF3)ppy = 2-(2,4-difluorophenyl)-5-(trifluoromethyl)pyridine] bridging ligands and vertically terminating the SBUs with catalytic Ni(MBA)Cl-2 [MBA = 2-(4' -methyl-[2,2'-bipyridin]-4-yl)acetate] capping agents. Hf-12-Ir-Ni was synthesized in a bottom-up approach and characterized by TEM, AFM, PXRD, TGA, NMR, ICP-MS, UV-vis, and luminescence spectroscopy. The proximity between photosensitizing Ir centers and catalytic Ni centers (similar to 0.85 nm) in Hf-12-Ir-Ni facilitates single electron transfer, leading to a 15-fold increase in photoredox reactivity. Hf-12-Ir-Ni was highly effective in catalytic C-S, C-O, and C-C cross-coupling reactions with broad substrate scopes and turnover numbers of similar to 4500, similar to 1900, and similar to 450, respectively.
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