4.8 Article

Structural elucidation of supported Rh complexes derived from RhCl (PPh3)3 immobilized on surface-functionalized SBA-15 and their catalytic performance for C-heteroatom (S, O) bond formation

期刊

JOURNAL OF CATALYSIS
卷 365, 期 -, 页码 43-54

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2018.06.012

关键词

Rhodium; Wilkinson's catalyst; Surface organometallic catalyst; Nuclear magnetic resonance; Extended X-ray absorption spectroscopy; Hydrothiolation; Hydrosulfonation; Stereoselectivity

资金

  1. Department of Energy, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Sciences Program [DE-SC0016192]
  2. DOE Office of Science [DE-AC02-06CH11357]
  3. Qingdao Institute of Bioenergy and Bioprocess Technology (QIBEBT), Chinese Academy of Sciences [Y6710619KL]
  4. U.S. Department of Energy (DOE) [DE-SC0016192] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

The local structures of rhodium complexes derived from the immobilization of Wilkinson's complex, RhCI (PPh3)(3), on SBA-15 silica functionalized with primary-amine, secondary-amine, or diphenylphosphine groups within the mesoporous channels were characterized by a series of techniques including XRD, HR-TEM, multinuclear ((13)c/(29)si/P-31) solid-state NMR, 2D P-31{H-1) HETCOR NMR, XPS, and Rh K-edge EXAFS. Immobilization of RhCI(PPh3)(3) through covalent bond formation with different functional groups grafted to the silica surface lead to variations in the local structure of the Rh center that has important implications for catalysis. The immobilized Rh complexes demonstrated high activity for the addition of alkynes with thiols (hydrothiolation) or sulfonic acids (hydrosulfonation) with excellent regio- and stereoselectivity under mild reaction conditions. This work demonstrates the elucidation of the local structure of the immobilized Rh complexes requires a complimentary multi-technique characterization approach that probes both the metal center itself and surrounding ligands. (C) 2018 Elsevier Inc. All rights reserved.

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