Self-assembly of amphiphilic alternating copolymers with stimuli-responsive rigid pendant groups

被引:12
作者
Lv, Yisheng [1 ]
Wang, Liquan [1 ]
Liu, Fan [1 ]
Feng, Weisheng [1 ]
Wei, Jie [1 ]
Lin, Shaoliang [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Key Lab Ultrafine Mat,Sch Mat Sci & Engn, Minist Educ,Shanghai Key Lab Adv Polymer Mat, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLECULAR-DYNAMICS SIMULATION; POLYMER; VESICLES; MORPHOLOGY; MICELLES; BRUSHES;
D O I
10.1039/d0py00765j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic alternating copolymers (AACs) possess unique self-assembly behaviours owing to their unique regular architecture. In this work, we employed dissipative particle dynamics simulations to explore the self-assembly behaviours of AACs with rigid pendants in selective solvents. The effects of block lengths and copolymer concentrations on the morphology of aggregates were examined. Two morphology diagrams were mapped out to provide a comprehensive understanding of the effect of these factors. The self-assembly process and the structure of aggregates were analysed in detail. The result shows that the amphiphilic alternating architecture can dramatically disturb the tendency of the ordered arrangement of rigid blocks. Furthermore, a rod-to-coil conformation transition of rigid blocks was performed to investigate the stimuli-responsive self-assembly behaviours. A comparison between the simulation results and our previous experimental observations was made, and the agreement is achieved.
引用
收藏
页码:4798 / 4806
页数:9
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