Abstract

The synthesis of well-defined block copolymers from one-pot monomer mixtures is particularly challenging when monomers are from the same class and show similar reactivity. Herein, an indium-based catalyst that shows comparable rates in the ring-opening homopolymerization of β-butyrolactone (β-BL) and ε-decalactone (ε-DL), demonstrates monomer-selective behavior in one-pot copolymerizations of β-BL and ε-DL. This provides simple and rapid access to well-defined di-, tri-, or tetra-block copolyesters from monomer mixtures. The sequence-controlled nature of these polymers was confirmed by kinetic analysis, 13C{1H} NMR spectroscopy, DSC, and TGA measurements.

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