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Cobalt-Catalyzed Regiodivergent Double Hydrosilylation of Arylacetylenes.
Cheng, Zhaoyang; Li, Minghua; Zhang, Xu-Yang; Sun, Yue; Yu, Qing-Lei; Zhang, Xing-Hong; Lu, Zhan.
Afiliação
  • Cheng Z; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Li M; Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
  • Zhang XY; Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Sun Y; Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Yu QL; Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Zhang XH; Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
  • Lu Z; Center of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University, Hangzhou, 310027, China.
Angew Chem Int Ed Engl ; 62(1): e202215029, 2023 Jan 02.
Article em En | MEDLINE | ID: mdl-36330602
ABSTRACT
Double hydrosilylation of alkynes represents a straightforward method to synthesize bis(silane)s, yet it is challenging if α-substituted vinylsilanes act as the intermediates. Here, a cobalt-catalyzed regiodivergent double hydrosilylation of arylacetylenes is reported for the first time involving this challenge, accessing both vicinal and geminal bis(silane)s with exclusive regioselectivity. Various novel bis(silane)s containing Si-H bonds can be easily obtained. The gram-scale reactions could be performed smoothly. Preliminarily mechanistic studies demonstrated that the reactions were initiated by cobalt-catalyzed α-hydrosilylation of alkynes, followed by cobalt-catalyzed ß-hydrosilylation of the α-vinylsilanes to deliver vicinal bis(silane)s, or hydride-catalyzed α-hydrosilylation to give geminal ones. Notably, these bis(silane)s can be used for the synthesis of high-refractive-index polymers (nd up to 1.83), demonstrating great potential utility in optical materials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China