117776-17-7Relevant articles and documents
Isolation of a Cyclopentasilane from Magnesium Reduction of a Linear Hexasilane
Ballestero-Martínez, Ernesto,Ferguson, John T.,Siegler, Maxime A.,Klausen, Rebekka S.
, p. 4641 - 4646 (2021)
The reductive cyclization of two linear hexasilanes is contrasted, where a methylated precursor yielded a cyclohexasilane while the tert-butyl-functionalized analog unexpectedly yielded a cyclopentasilane. A comprehensive analysis using X-ray diffraction, IR, HR, HRMS, and multinuclear (1H, 13C and 29Si) 1D and 2D NMR spectroscopy identified the 1,2-dihydrodisilane tBuPhHSi-SiHPhtBu as an additional product, which was interpreted as supportive of a mechanism involving silylene elimination. The results of this study may prove informative about substituent effects in the practice of complex organosilicon molecular synthesis.