Electron-Induced Conversion of Silylones to Six-Membered Cyclic Silylenes

被引:22
|
作者
Roy, Sudipta [1 ]
Mondal, Kartik Chandra [1 ]
Krause, Lennard [1 ]
Stollberg, Peter [1 ]
Herbst-Irmer, Regine [1 ]
Stalke, Dietmar [1 ]
Meyer, Jann [1 ]
Stueckl, A. Claudia [1 ]
Maity, Bholanath [2 ]
Koley, Debasis [2 ]
Vasa, Suresh Kumar [3 ]
Xiang, Sheng Qi [3 ]
Linser, Rasmus [3 ]
Roesky, Herbert W. [1 ]
机构
[1] Univ Gottingen, Inst Anorgan Chem, D-37077 Gottingen, Germany
[2] IISER Kolkata, Dept Chem Sci, Mohanpur 741252, India
[3] Max Planck Inst Biophys Chem, Abt NMR Basierte Strukturbiol, D-37077 Gottingen, Germany
关键词
COORDINATION CHEMISTRY; SILICON(0); CARBODICARBENE; SILADICARBENE; BONDS;
D O I
10.1021/ja510427r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A silicon atom in the zero oxidation state stabilized by two carbene ligands is known as siladicarbene (silylone). There are two pairs of electrons on the silicon atom in silylone. This was recently confirmed by both experimental and theoretical charge density investigations. The silylone is stable up to 195 degrees C in an inert atmosphere. However, a substoichiometric amount (33 mol%) of potassium metal triggers the activation of the unsaturated C:Si:C backbone, leading to a selective reaction with a tertiary C-H bond in an atom-economical approach to form a six-membered cyclic silylene with three-coordinate silicon atom. Cyclic voltammetry shows that this reaction proceeds via the formation of a silylone radical anion intermediate, which is further confirmed by EPR spectroscopy.
引用
收藏
页码:16776 / 16779
页数:4
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