聚合物
单体
解聚
聚合
材料科学
区域选择性
结晶度
复分解
高分子科学
高分子化学
合理设计
有机化学
化学
化学结构
化学工程
化学改性
开环复分解聚合
支化(高分子化学)
共聚物
嫁接
热稳定性
立体选择性
作者
Yi Wang,Jianhua Tang,Yiyang Liang,Zhenyang Luo,Yucheng He,Puyou Jia,Xu E,Ye Sha
摘要
Chemically recyclable polymers that depolymerize back to their monomers offer a promising alternative to non‑recyclable petroleum‑based plastics. However, three seemingly intractable trade‑offs have long hindered the rational design of circular polymers that combine high chemical recyclability with high performance: polymerizability versus depolymerizability, depolymerizability versus material performance, and crystallinity versus ductility. Here, we introduce a monomer design strategy based on renewable cyclic enoates that enables highly regioselective (exclusive head‑to‑tail) and stereoselective (E‑selective) ring‑opening metathesis polymerization (ROMP), yielding polyolefins/polyesters with high crystallinity and full chemical recyclability. Through modulation of the ring-chain equilibrium, both the forward polymerization and the reverse depolymerization proceeded to near-quantitative conversion. These polymers defy the aforementioned trade‑offs by exhibiting an unusual combination of desirable properties, including intrinsic crystallinity, chemical recyclability, and excellent performance metrics such as high thermal stability, high mechanical strength, ductility, and toughness.
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