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Recent progress in transition metal complexes featuring silylene as ligands.
Hendi, Zohreh; Pandey, Madhusudan K; Kushvaha, Saroj Kumar; Roesky, Herbert W.
Afiliação
  • Hendi Z; Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Göttingen, 37077, Germany. hroesky@gwdg.de.
  • Pandey MK; Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Göttingen, 37077, Germany. hroesky@gwdg.de.
  • Kushvaha SK; Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Göttingen, 37077, Germany. hroesky@gwdg.de.
  • Roesky HW; Institut für Anorganische Chemie, Georg-August-Universität Göttingen, Göttingen, 37077, Germany. hroesky@gwdg.de.
Chem Commun (Camb) ; 60(71): 9483-9512, 2024 Aug 29.
Article em En | MEDLINE | ID: mdl-39119696
ABSTRACT
Silylenes, divalent silicon(II) compounds, once considered highly reactive and transient species, are now widely employed as stable synthons in main-group and coordination chemistry for myriad applications. The synthesis of stable silylenes represents a major breakthrough, which led to extensive exploration of silylenes in stabilizing low-valent main-group elements and as versatile ligands in coordination chemistry and catalysis. In recent years, the exploration of transition metal complexes stabilized with silylene ligands has captivated significant research attention. This is due to their robust σ-donor characteristics and capacity to stabilize transition metals in low valent states. It has also been demonstrated that the transition metal complexes of silylenes are effective catalysts for hydroboration, hydrosilylation, hydrogenation, hydrogen isotope exchange reactions, and small molecule activation chemistry. This review article focuses on the recent progress in the synthesis and catalytic application of transition metal complexes of silylenes.

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