Ring-opening polymerization of cyclic oligosiloxanes without producing cyclic oligomers
Li-Miao Shi, Aurélie Boulègue-Mondière, Delphine Blanc, Antoine Baceiredo, Vicenç Branchadell, Tsuyoshi Kato
Abstract
A long-standing problem associated with silicone synthesis is contamination of the polymer products with 10 to 15% cyclic oligosiloxanes that results from backbiting reactions at the polymer chain ends. This process, in competition with chain propagation through ring-opening polymerization (ROP) of cyclic monomers, was thought to be unavoidable and routinely leads to a thermodynamically controlled reaction mixture (polymer/cyclic oligosiloxanes = 85/15). Here, we report that simple alcohol coordination to the anionic chain ends prevents the backbiting process and that a well-designed phosphonium cation acts as a self-quenching system in response to loss of coordinating alcohols to stop the reaction before the backbiting process begins. The combination of both effects allows a thermodynamically controlled ROP of the eight-membered siloxane ring D 4 without producing undesirable cyclic oligosiloxanes.