By-Product-Free Siloxane-Bond Formation and Programmed One-Pot Oligosiloxane Synthesis

Angew Chem Int Ed Engl. 2017 Mar 13;56(12):3168-3171. doi: 10.1002/anie.201611623. Epub 2017 Feb 2.

Abstract

Siloxane bonds are usually synthesized by condensation reactions, such as hydrolysis/dehydration and cross-coupling reactions, in which the generation of by-products during bond formation can not be avoided. We have developed a one-pot sequence of iridium-catalyzed silyl ester hydrosilylation and boron-catalyzed rearrangement of the resulting disilyl acetals for the construction of siloxane bonds, in principle without the formation of any by-products. Moreover, the programmed synthesis of tri-, tetra-, and pentasiloxanes was possible in a single flask by combining the above sequence of iridium-catalyzed hydrosilylation and boron-catalyzed rearrangement with a boron-catalyzed cross-coupling reaction. The obtained oligosiloxanes are difficult to synthesize selectively by other known synthetic procedures.

Keywords: boron catalysis; hydrosilylation; rearrangement; silanes; siloxanes.

Publication types

  • Research Support, Non-U.S. Gov't