Synthesis of an NHC-Coordinated Dialkyldisilavinylidene and Its Oxidation Providing a Silicon Analog of an Acetolactone
Ryo Kobayashi, Shintaro Ishida, Takeaki Iwamoto
Abstract
Although isolable silicon analogs of acetylene have been extensively studied, the silicon analogs of vinylidene, which is a short-lived isomer of acetylene, remain scarce. Herein, we report isolable NHC-coordinated dialkyldisilavinylidene 1 synthesized by the reduction of a tetrabromodisilane featuring a bulky alkyl protecting group. 1 was fully characterized by a combination of multinuclear NMR spectroscopy, high-resolution mass spectrometry, elemental analysis, and X-ray diffraction analysis. The UV–vis spectrum and DFT calculations disclosed that 1 possesses an Si═Si double bond and lone pair electrons on the terminal Si atom coordinated by the NHC. 1 reacted with N2O and B(C6F5)3 to provide a silicon analog of an acetolactone stabilized by a Lewis base and a Lewis acid (4).