Advancing the Development of Recyclable Aromatic Polyesters by Functionalization and Stereocomplexation

The development of innovative synthetic polymer systems to overcome the trade-offs between the polymer's depolymerizability and performance properties is in high demand for advanced material applications and sustainable development. In this contribution, we prepared a class of aromatic cyclic esters (M1-M5) from thiosalicylic acid and epoxides by facile one-pot synthesis. Ring-opening polymerization of Ms afforded aromatic polyesters P(M)s with high molecular weights and narrow dispersities. The physical and mechanical properties of P(M)s can be modulated by stereocomplexation and regulation of the side-chain flexibility of the polymers, ultimately achieving high-performance properties such as high thermal stability and crystallinity (T-m up to 209 degrees C), as well as polyolefin-like high mechanical strength, ductility, and toughness. Furthermore, the functionalizable moieties of P(M)s have driven a wide array of post-polymerization modifications toward access to value-added materials. More importantly, the P(M)s were able to selectively depolymerize into monomers in excellent yields, thus establishing its circular life cycle.

Automated summary

This contribution focuses on the development of innovative synthetic polymer systems for advanced material applications and sustainable development. Aromatic polyesters were successfully prepared through a facile one-pot synthesis and showed high-performance properties such as high thermal stability, crystallinity, mechanical strength, ductility, and toughness. The functionalizable moieties of the polyesters allowed for post-polymerization modifications and the polymers exhibited excellent circular life cycle through selective depolymerization into monomers.