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Towards ligand simplification in manganese-catalyzed hydrogenation and hydrosilylation processes

期刊

COORDINATION CHEMISTRY REVIEWS
卷 458, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2022.214421

关键词

Manganese complexes; Bidentate ligands; Hydrogenation; Transfer Hydrogenation; Hydrogen borrowing; Hydrosilylation

资金

  1. Centre National de la Recherche Scientifique (CNRS)
  2. Russian Science Foundation [20-73-00311]
  3. Universite Toulouse III Paul Sabatier
  4. Institut Universi-taire de France (IUF)
  5. Embassy of Yemen in Paris
  6. program Pause
  7. French Embassy in Moscow
  8. Russian Science Foundation [20-73-00311] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

This paper provides a comprehensive review of the rapidly emerging application of organometallic manganese complexes in catalytic reactions. It focuses on the influence of different donor ligands on catalytic activity and selectivity, the comparison with polydentate systems, and the study of mechanistic aspects.
Rapidly emerging application of organometallic manganese complexes incorporating less elaborated mono- and bidentate donor ligands in catalytic hydrogenation, transfer hydrogenation, hydrogenborrowing and hydrosilylation processes is comprehensively reviewed. Special attention is devoted to the influence of the nature of donor moieties (P-, N- and C-donors) on the catalytic activity and/or selectivity, the comparison with structurally related polydentate systems and mechanistic aspects.CO 2022 Elsevier B.V. All rights reserved.

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