A photo-thermal dual-regulated latent monomer strategy for sequence control of polymers

被引:6
作者
Zhang, Liuqiao [1 ]
Song, Yuyang [1 ]
Cao, Yuhang [1 ]
Wang, Zhen [1 ]
Huang, Zhihao [1 ]
Xuan, Sunting [1 ]
Zhang, Zhengbiao [1 ,2 ]
机构
[1] Soochow Univ, State & Local Joint Engn Lab Novel Funct Polymer, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Soochow Univ, State Key Lab Radiat Med & Protect, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
ITERATIVE EXPONENTIAL-GROWTH; RADICAL POLYMERIZATION; TRIBLOCK COPOLYMERS; PHENYL MALEIMIDE; ETHYL; METHACRYLATE; TRANSITION;
D O I
10.1039/d1py00961c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Sequence-control, widely found in biopolymers (e.g., DNA), remains a significant challenge in polymer synthesis. Here, the concept of the photo-thermal dual-regulated release of the methyl maleimide (MMI) monomer in RAFT copolymerizations is presented, aiming to enrich the current methodologies of polymer sequence control. Photo-sensitive dithienylfuran-protected methyl maleimide (DTFMMI) was used as a latent monomer in which the dithienyl groups were in the "ring-closed" form under ultraviolet irradiation. This rigid structure significantly reduced its activity towards the retro Diels-Alder (rDA) reaction and the monomer remained dormant at a high temperature. However, the dithienyl group transformed to its "ring-open" analogue with the irradiation of visible light and triggered the rDA reaction of DTFMMI, allowing the release of active MMI and its gradual incorporation into the growing polymer chains. As a result, the structural isomerization of DTFMMI and the onset release of MMI could be well controlled by light and temperature, collectively, to regulate the polymer sequence in a more facile and non-invasive way. This proof-of-concept study sheds light on the development of synthetic methods for the construction of more advanced sequence-controlled polymers.
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页码:4996 / 5002
页数:7
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