详细信息
Lifecycle of dynamic covalent polar-olefin macrocycles via entropy-driven ring-opening polymerization and closed-loop chemical recycling
文献类型:期刊文献
中文题名:Lifecycle of dynamic covalent polar-olefin macrocycles via entropy-driven ring-opening polymerization and closed-loop chemical recycling
作者:Pengyun Li[1];Chong Li[1];Mengying Lei[1];Ruirui Gu[1];He Tian[1];Da-Hui Qu[1]
机构:[1]Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering,Feringa Nobel Prize Scientist Joint Research Center,Frontiers Science Center for Materiobiology and Dynamic Chemistry,Institute of Fine Chemicals,School of Chemistry and Molecular Engineering,East China University of Science and Technology,Shanghai 200237,China
年份:2025
卷号:12
期号:12
起止页码:80
中文期刊名:National Science Review
外文期刊名:国家科学评论(英文版)
基金:supported by the National Natural Science Foundation of China(22025503,22588101,22571084,22205064 and 22220102004);the Science and Technology Commission of Shanghai Municipality(24DX1400200);the Innovation Program of Shanghai Municipal Education Commission(2023ZKZD40);the Programme of Introducing Talents of Discipline to Universities(B16017);the Fundamental Research Funds for the Central Universities;the CNPC Innovation Found(2024DQ02-0410).
语种:英文
中文关键词:dynamic covalent chemistry;polar olefin bonds;entropy-driven ring-opening polymerization;closed-loop chemical recycling
摘要:The global plastic pollution crisis urgently demands closed-loop chemical recycling strategies.While recyclable polymers via olefin metathesis have been widely explored,the development of metal-free methods operating under mild conditions remains a significant challenge.Here,we present the lifecycle design of polar-olefin-derived macrocycles as novel monomers capable of undergoing reversible entropy-driven ring-opening polymerization(ED-ROP)through organic base-catalyzed metathesis of polar olefin bonds.High-molecular-weight polymers were efficiently produced via bulk melt polymerization.Kinetic studies and mass analyses indicated the formation of cyclic polymer topologies through insertion and ring expansion,with polymerization thermodynamically driven by an increase in conformational entropy.By shifting the equilibrium of polar-olefin metathesis in dilute solution,these polymers enable efficient closed-loop depolymerization and monomer recovery.This approach establishes a versatile platform based on polar olefin chemistry,advancing the design of recyclable materials with tailored dynamic functionalities.
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