Synthesis and Functionalization of a 1,4-Bis(trimethylsilyl)tetrasila-1,3-diene through the Selective Cleavage of Si(sp²)–Si(sp³) Bonds under Mild Reaction Conditions

Abstract

Although the oxidative coupling of disilenides, i.e., the disilicon analogues of vinyl anions, represents a promising route to extend the conjugation between SiSi double bonds, previously reported synthetic routes to disilenides involve strongly reducing conditions. Herein, we report a novel synthetic route to disilenides from stable disilenes via the selective cleavage of Si­(sp²)–Si­(sp³) bonds under milder reaction conditions. Using this method, a 1,4-bis­(trimethylsilyl)­tetrasila-1,3-diene (<b>5</b>) was synthesized from the corresponding silyl-substituted disilene. Moreover, Et₃Si-substituted tetrasila-1,3-diene <b>7</b> was synthesized via tetrasila-1,3-dien-1-ide <b>6</b>, which is the first example of a functionalized tetrasila-1,3-diene