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Tetrasila-1,3-butadiene and its transformation to disilenyl anions

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Silicon Chemistry

Abstract

The reaction of dilithiosilane, (tBu2MeSi)2SiLi2 (2), with 1,1,2,2-tetrachloro-1,2-dimesityldisilane produced the tetrasila-1,3-butadiene derivative, (tBu2MeSi)2Si=Si(Mes)–(Mes)Si=Si(SiMetBu2)2 (3, Mes = 2,4,6-trimethyl-phenyl), which was isolated as reddish-purple crystals. The structure of 3 was determined by both spectroscopic and crystallographic methods; the Si=Si double bond lengths are 2.2003(12) and 2.1983(12) Å, and the length of the central Si−Si single bond is 2.3376(11) Å. The tetrasilabutadiene moiety is highly twisted, the torsional angle of Si1=Si2−Si3=Si4 being 72°. The reaction of 3 with tBuLi or KC8 in THF gave the disilenyllithium 4 and disilenylpotassium 5, which contain an sp 2-type silyl anion, by the reductive cleavage of the central Si–Si bond in 3.

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Correspondence to Akira Sekiguchi.

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Dedicated to Professor Mitsuo Kiro on the occasion of his 2005 Wacker Award and in recognition of his outstanding contribution to silicon chemistry.

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Ichinohe, M., Sanuki, K., Inoue, S. et al. Tetrasila-1,3-butadiene and its transformation to disilenyl anions. Silicon Chem 3, 111–116 (2007). https://doi.org/10.1007/s11201-006-9011-x

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  • DOI: https://doi.org/10.1007/s11201-006-9011-x

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