One-Electron-Mediated Rearrangements of 2,3-Disiladicarbene

Kartik Chandra Mondal, Prinson P. Samuel, Herbert W. Roesky, Rinat R. Aysin, L. A. Leites, Sven Neudeck, Jens Lübben, Birger Dittrich, Nicole Holzmann, Markus Hermann,

Journal of the American Chemical Society · 2014 · 83 citations · 28 references

Concepts

Abstract

A disiladicarbene, (Cy-cAAC)2Si2 (2), was synthesized by reduction of Cy-cAAC:SiCl4 adduct with KC8. The dark-colored compound 2 is stable at room temperature for a year under an inert atmosphere. Moreover, it is stable up to 190 °C and also can be characterized by electron ionization mass spectrometry. Theoretical and Raman studies reveal the existence of a Si═Si double bond with a partial double bond between each carbene carbon atom and silicon atom. Cyclic voltammetry suggests that 2 can quasi-reversibly accept an electron to produce a very reactive radical anion, 2(•-), as an intermediate species. Thus, reduction of 2 with potassium metal at room temperature led to the isolation of an isomeric neutral rearranged product and an anionic dimer of a potassium salt via the formation of 2(•-).

References

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