A Polycondensation–depolymerization strategy enables closed-loop recyclable polyoxalates <i>via</i> ring-opening polymerization of six-membered cyclic oxalates

Developing a simple and efficient strategy for the scalable production of closed-loop recyclable polymers from abundant and low-cost feedstocks remains highly desirable. Here, we present a facile "polycondensation-depolymerization" approach for the large-scale synthesis of cyclic 1,2-alkylene oxalates, which undergo controlled ring-opening polymerization to yield high-molecular-weight polyoxalates. The influence of alkyl substituents on the polymerization kinetics, thermodynamics, and material properties was systematically investigated. Remarkably, these polyoxalates can be chemically recycled to their pristine monomers with high purity and yield using sodium glycolate as a catalyst. Furthermore, the polyoxalates exhibit excellent marine degradability, providing a promising strategy to tailor the seawater degradation behavior of polyesters through copolymerization.

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Publication Details

Journal
Chemical Science
Published
2025-12-22
DOI
https://doi.org/10.1039/d5sc08361c
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

A Polycondensation–depolymerization strategy enables closed-loop recyclable polyoxalates via ring-opening polymerization of six-membered cyclic oxalates

Dongfang Zhao, Z. X. Li, Zheng Li, Yong Shen et al.
Chemical Science
Carbon dioxide utilization in catalysis
article

A Polycondensation–depolymerization strategy enables closed-loop recyclable polyoxalates via ring-opening polymerization of six-membered cyclic oxalates

Dongfang Zhao, Z. X. Li, Zheng Li, Yong Shen, Yalei Liu
article en

Abstract

Developing a simple and efficient strategy for the scalable production of closed-loop recyclable polymers from abundant and low-cost feedstocks remains highly desirable. Here, we present a facile "polycondensation-depolymerization" approach for the large-scale synthesis of cyclic 1,2-alkylene oxalates, which undergo controlled ring-opening polymerization to yield high-molecular-weight polyoxalates. The influence of alkyl substituents on the polymerization kinetics, thermodynamics, and material properties was systematically investigated. Remarkably, these polyoxalates can be chemically recycled to their pristine monomers with high purity and yield using sodium glycolate as a catalyst. Furthermore, the polyoxalates exhibit excellent marine degradability, providing a promising strategy to tailor the seawater degradation behavior of polyesters through copolymerization.

Chemical ScienceVol. 17(7)
Qingdao University of Science and Technology (CN), State Key Laboratory of Chemical Engineering (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 47%
Carbon dioxide utilization in catalysis
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