木筏
共聚物
可逆加成-断裂链转移聚合
链式转移
聚合
高分子化学
材料科学
聚合物囊泡
化学
聚合物
两亲性
自由基聚合
复合材料
作者
Ruiming Zeng,Ying Chen,Li Zhang,Jianbo Tan
出处
期刊:Macromolecules
[American Chemical Society]
日期:2020-02-25
卷期号:53 (5): 1557-1566
被引量:48
标识
DOI:10.1021/acs.macromol.0c00123
摘要
Reversible addition-fragmentation chain transfer (RAFT)-mediated polymerization-induced self-assembly (PISA) has served as a versatile platform for the large-scale preparation of block copolymer nano-objects with a diverse set of morphologies. However, almost all PISA formulations are focused on the syntheses of linear block copolymers rather than star block copolymers. Owing to the asymmetrical structure of the RAFT agent, herein, we report a direct comparison between Z-RAFT (the nonfragmenting group attached to the core) and R-RAFT (the fragmenting group attached to the core) strategies for preparing well-defined star block copolymer nano-objects via RAFT-mediated PISA. We showed that the Z-RAFT strategy is a more suitable strategy for the preparation of star block copolymer nano-objects without compromising the control over the molecular weight and morphology. A binary mixture of Z-type and R-type tetrafunctional macro-RAFT agents was used to control the morphologies of star block copolymer assemblies. The effect of numbers of the RAFT group on polymerization kinetics and morphologies of block copolymer nano-objects was also investigated in detail. Finally, (ABC)4 four-arm star triblock copolymer vesicles were prepared by seeded RAFT dispersion polymerization of solvophobic and solvophilic monomers using (AB)4 four-arm star diblock copolymer vesicles as seeds. This research not only expands the scope for preparing well-defined star block copolymer nano-objects but also provides important insights into the effect of the polymer architecture on RAFT-mediated PISA.
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