RAFT Step-Growth Polymerization of Diacrylates

被引:23
作者
Archer, Noel E. [1 ]
Boeck, Parker T. [1 ]
Ajirniar, Yasmin [1 ]
Tanaka, Joji [1 ]
You, Wei [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
FRAGMENTATION CHAIN TRANSFER; MEDIATED POLYMERIZATION; RADICAL POLYMERIZATION; BLOCK-COPOLYMERS; INITIALIZATION; KINETICS;
D O I
10.1021/acsmacrolett.2c00476
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
RAFT step-growth polymerization was previously demonstrated with monomers that bear low rate of homopropa-gation 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.
引用
收藏
页码:1079 / 1084
页数:6
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