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Catalytic hydrogenation of olefins by a multifunctional molybdenum-sulfur complex.
Xue, Minghui; Peng, Zhiqiang; Tao, Keyan; Jia, Jiong; Song, Datong; Tung, Chen-Ho; Wang, Wenguang.
Afiliação
  • Xue M; School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, China.
  • Peng Z; College of Chemistry, Beijing Normal University, 100875, Beijing, China.
  • Tao K; College of Chemistry, Beijing Normal University, 100875, Beijing, China.
  • Jia J; School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, China.
  • Song D; Davenport Chemical Research Laboratories, Department of Chemistry, University of Toronto, Toronto, ON, M5S 3H6, Canada. d.song@utoronto.ca.
  • Tung CH; School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, China.
  • Wang W; School of Chemistry and Chemical Engineering, Shandong University, 250100, Jinan, China. wwg@bnu.edu.cn.
Nat Commun ; 15(1): 797, 2024 Jan 27.
Article em En | MEDLINE | ID: mdl-38280870
ABSTRACT
Exploration of molybdenum complexes as homogeneous hydrogenation catalysts has garnered significant attention, but hydrogenation of unactivated olefins under mild conditions are scarce. Here, we report the synthesis of a molybdenum complex, [Cp*Mo(Ph2PC6H4S-CH = CH2)(Py)]+ (2), which exhibits intriguing reactivity toward C2H2 and H2 under ambient pressure. This vinylthioether complex showcases efficient catalytic activity in the hydrogenation of various aromatic and aliphatic alkenes, demonstrating a broad substrate scope without the need for any additives. The catalytic pathway involves an uncommon oxidative addition of H2 to the cationic Mo(II) center, resulting in a Mo(IV) dihydride intermediate. Moreover, complex 2 also shows catalytic activity toward C2H2, leading to the production of polyacetylene and the extension of the vinylthioether ligand into a pendant triene chain.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article