Living Cationic Ring-Opening Polymerization of Hetero Diels-Alder Adducts to Give Multifactor-Controlled and Fast-Photodegradable Vinyl Polymers

被引:6
作者
Chae, Ju-Hyung [1 ]
Choi, Minyeong [1 ]
Son, Semin [1 ]
Ko, Su-Min [1 ]
Lee, In-Hwan [2 ]
机构
[1] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea
[2] Ajou Univ, Dept Chem, Suwon 16499, South Korea
基金
新加坡国家研究基金会;
关键词
Alternating; Hetero Diels-Alder Adduct; Living Polymerization; Photodegradation; Ring-Opening; ENOL SILYL ETHERS; RADICAL POLYMERIZATION; METATHESIS POLYMERIZATION; COPOLYMERS; SEQUENCE; ACETALS; PHOTOCHEMISTRY; SCISSION; KETONE);
D O I
10.1002/anie.202305414
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Precise control of multiple structural parameters associated with vinyl polymers is important for producing materials with the desired properties and functions. While the development of living polymerization methods has provided a way to control the various structural parameters of vinyl polymers, the concomitant control of their sequence and regioregularity remains a challenging task. To overcome this challenge, herein, we report the living cationic ring-opening polymerization of hetero Diels-Alder adducts. The scalable and modular synthesis of the cyclic monomers was achieved by a one-step protocol using readily available vinyl precursors. Subsequently, living polymerization of the cyclic monomers was examined, allowing the synthesis of vinyl polymers while controlling multiple factors, including molecular weight, dispersity, alternating sequence, head-to-head regioregularity, and end-group functionality. The living characteristics of the developed method were further demonstrated by block copolymerization. The synthesized vinyl polymers exhibited unique thermal properties and underwent fast photodegradation even under sunlight.
引用
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页数:8
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