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Issue 24, 2017
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Disilametallacyclic chemistry for efficient catalysis

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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 H2Pt(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.

Graphical abstract: Disilametallacyclic chemistry for efficient catalysis

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Article information

10 Apr 2017
25 May 2017
First published
26 May 2017

Dalton Trans., 2017,46, 7644-7655
Article type

Disilametallacyclic chemistry for efficient catalysis

Y. Sunada and H. Nagashima, Dalton Trans., 2017, 46, 7644
DOI: 10.1039/C7DT01275F

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