木筏
链式转移
聚合
单体
可逆加成-断裂链转移聚合
丙烯酸酯
高分子化学
双功能
材料科学
聚合物
化学
自由基聚合
有机化学
催化作用
作者
Noel E. Archer,Parker T. Boeck,Yasmin Ajirniar,Joji Tanaka,Wei You
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2022-08-19
卷期号:11 (9): 1079-1084
被引量:21
标识
DOI:10.1021/acsmacrolett.2c00476
摘要
RAFT step-growth polymerization was previously demonstrated with monomers that bear low rate of homopropagation to favor the chain transfer process; by contrast, acrylates are known to be fast homopropagating monomers, thereby posing serious challenges for RAFT step-growth. Here, we identified a chain transfer agent (CTA) that rapidly yields single unit monomer inserted (SUMI) CTA adducts with a model acrylate monomer. Using a bifunctional reagent of this CTA, we successfully demonstrated RAFT step-growth polymerization with diacrylates, yielding linear polymer backbones. Furthermore, we achieved inclusion of functionality (i.e., disulfide) into RAFT step-growth polymer via a disulfide incorporated bifunctional CTA. Grafting from this backbone resulted in molecular brush polymers with cleavable functionality in each repeat unit of the backbone, allowing selective degradation to afford well-defined unimolecular species of two polymeric side chains. Given the wide selection of commercially available diacrylates, RAFT step-growth polymerization of diacrylates will further enable facile synthesis of complex architectures with modular backbones.
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