木筏
链式转移
可逆加成-断裂链转移聚合
聚合
单体
高分子化学
材料科学
链生长聚合
乳液聚合
阳离子聚合
沉淀聚合
化学工程
本体聚合
化学
自由基聚合
聚合物
有机化学
工程类
作者
Zhou Jiaxi,Qian Huang,Li Zhang,Jianbo Tan
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2023-10-16
卷期号:12 (11): 1457-1465
被引量:9
标识
DOI:10.1021/acsmacrolett.3c00547
摘要
We exploited the monomer-feeding mechanism of reversible addition–fragmentation chain transfer (RAFT) emulsion polymerization to achieve the successful polymerization-induced self-assembly (PISA) of asymmetric divinyl monomers. Colloidally stable cross-linked block copolymer nanoparticles with various morphologies, such as vesicles, were directly prepared at high solids. Morphologies of the cross-linked block copolymer nanoparticles could be controlled by varying the monomer concentration, degree of polymerization (DP) of the core-forming block, and length of the macro-RAFT agent. X-ray photoelectron spectroscopy (XPS) characterization confirmed the presence of unreacted vinyl groups within the obtained block copolymer nanoparticles, providing a landscape for further functionalization via thiol–ene chemistry. Finally, the obtained block copolymer nanoparticles were employed as additives to tune the mechanical properties of hydrogels. We expect that this study not only offers considerable opportunities for the preparation of well-defined cross-linked block copolymer nanoparticles, but also provides important insights into the controlled polymerization of multivinyl monomers.
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