Morphological Stabilization of Block Copolymer Worms Using Asymmetric Cross-Linkers during Polymerization-Induced Self-Assembly

被引:59
|
作者
Zhang, Baohua [1 ]
Lv, Xiaoqing [1 ]
Zhu, Anqi [1 ]
Zheng, Jinwen [1 ]
Yang, Yongqi [1 ]
An, Zesheng [1 ]
机构
[1] Shanghai Univ, Inst Nanochem & Nanobiol, Coll Environm & Chem Engn, Shanghai 200114, Peoples R China
基金
中国国家自然科学基金;
关键词
RAFT DISPERSION POLYMERIZATION; CORE-SHELL NANOGELS; IN-SITU SYNTHESIS; VESICLE-TO-WORM; RADICAL POLYMERIZATION; PHOTO-PISA; END-GROUP; NANOPARTICLES; OBJECTS; LINKING;
D O I
10.1021/acs.macromol.8b00246
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Block copolymer worm stabilization via cross linking during polymerization-induced self-assembly (PISA) is challenging. This is because block copolymer worms typically occupy a narrow regime in the phase diagram, and in situ cross linking may hinder a morphological transition from sphere to worm. In this work, in situ cross-linking of block copolymer worms during PISA was studied using three different asymmetric cross-linkers, each bearing a pair of double bonds with different reactivities. Specifically, ethanolic PISA syntheses targeting poly(2-(dimethylamino)ethyl methacrylate)-bpoly(benzyl methacrylate) diblock copolymer worms were investigated in the presence of vinyl methacrylate, allyl methacrylate, or 4-allyloxybenzyl methacrylate. The copolymerizations of benzyl methacrylate with the asymmetric cross-linkers underwent progressive branching to finally cross-linking of the block copolymer worms. While all the three asymmetric cross-linkers were able to cross-link worms, 4-allyloxybenzyl methacrylate with a structure mimicking benzyl methacrylate showed the best results with minimal perturbation to the worm morphology.
引用
收藏
页码:2776 / 2784
页数:9
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