Disilametallacyclic chemistry for efficient catalysis. Issue 24 (13th June 2017)

• Record Type: Journal Article
• Authors: Sunada, Yusuke; Nagashima, Hideo
• Is Part Of: Dalton transactions. Volume 46:Issue 24(2017)
• Page Start: 7644
• Page End: 7655
• Publication Date: 2017-06-13
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c7dt01275f
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Disilametallacyclic species of late transition metals behave as key intermediates for efficient catalytic reactions proceeding through new mechanisms. Abstract : This article discusses two new features of disilametallacyclic chemistry that contribute to the development of efficient catalytic reactions in organic synthesis. The first is disilametallacyclic intermediates in the hydrosilane reduction of carbonyl compounds. Experimental and theoretical studies on disilaplatinacycles suggested that the H2 Pt(iv )Si2 species generated by oxidative addition of 1, 2-bis(dimethylsilyl)benzene behaves as a highly reactive hydride to reduce amides to amines. This mechanism via disilametallacyclic intermediates explains the efficient hydrosilane reduction of carbonyl compounds with α, ω-bifunctional hydrosilanes catalyzed by other transition metals. The second is hydrogenation of alkenes by disilaferra- or disilaruthenacyclic complexes as catalyst precursors. A new mechanism not involving the conventional oxidative addition of H2 was suggested from DFT calculations, in which activation of the H–H bond occurs in the metal–silicon bond of the disilametallacyclic intermediate. Disilametallacyclic intermediates contribute to efficient catalytic reactions through this σ-CAM (σ-complex assisted mechanism) type mechanism.