Abstract

Polyester block polymers containing polylactide have garnered significant attention as renewable, degradable alternatives to traditional elastomers. However, the low glass transition of the PLA blocks limits the upper-use temperatures of the resulting elastomers. To improve the thermal performance, we explore a series of multiblock polyesters composed of poly(e-decalactone) (PDL) and poly(cyclohexene phthalate) (PCHPE). These materials are prepared using switchable polymerization catalysis followed by chain extension. The strategy involves (i) alternating ring-opening copolymerization (ROCOP) of cyclohexene oxide and phthalic anhydride, (ii) e-decalactone ring-opening polymerization (ROP), and (iii) diisocyanate coupling of the telechelic triblocks to increase molar mass. The resulting multiblock polyesters are amorphous, and the blocks are phase separated; glass transition temperatures are ∼−45 and 100 °C. They show thermal resistance to mass loss with Td5% ∼ 285 °C and higher upper use temperatures comp...

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