A Cation-Dependent Dual Activation Motif for Anionic Ring-Opening Polymerization of Cyclic Esters

Abstract

A new organocatalyst for the ring-opening polymerization of lactones has been identified. Under the tested conditions, the anions of 2,2′-bisindole promote fast, living polymerizations (as short as 10 ms) which are selective for chain elongation over transesterification (D ≤ 1.1). While structurally related to (thio)urea anion catalysts, anions of 2,2′-bisindole activate the monomer via the counterion rather than through hydrogen bonding. This new activation motif enables modulation of the polymerization rate by 2 orders of magnitude by changing the counterion.