Recent progress in polymerization-induced self-assembly: From the perspective of driving forces

被引:31
作者
Zhao, Zizhuo [1 ]
Lei, Shujing [1 ]
Zeng, Min [2 ]
Huo, Meng [1 ]
机构
[1] Zhejiang Sci Tech Univ, Dept Chem, Key Lab Surface & Interface Sci Polymer Mat Zhejia, Hangzhou 310018, Peoples R China
[2] Univ Warwick, Dept Chem, Coventry CV4 7AL, England
来源
AGGREGATE | 2024年 / 5卷 / 01期
基金
中国国家自然科学基金;
关键词
driving forces; electrostatic interactions; hydrogen bonding; hydrophobic interactions; polymerization-induced self-assembly; POLYION COMPLEX MICELLES; ONE-POT SYNTHESIS; RAFT DISPERSION POLYMERIZATION; COPOLYMER NANO-ASSEMBLIES; CHARGED BLOCK-COPOLYMERS; ELECTROSTATIC INTERACTIONS; RADICAL POLYMERIZATION; DRIVEN; VESICLES; CRYSTALLIZATION;
D O I
10.1002/agt2.418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymerization-induced self-assembly (PISA) enables the simultaneous growth and self-assembly of block copolymers in one pot and therefore has developed into a high-efficiency platform for the preparation of polymer assemblies with high concentration and excellent reproducibility. During the past decade, the driving force of PISA has extended from hydrophobic interactions to other supramolecular interactions, which has greatly innovated the design of PISA, enlarged the monomer/solvent toolkit, and endowed the polymer assemblies with intrinsic dynamicity and responsiveness. To unravel the important role of driving forces in the formation of polymeric assemblies, this review summarized the recent development of PISA from the perspective of driving forces. Motivated by this goal, here we give a brief overview of the basic principles of PISA and systematically discuss the various driving forces in the PISA system, including hydrophobic interactions, hydrogen bonding, electrostatic interactions, and & pi;-& pi; interactions. Furthermore, PISA systems that are driven and regulated by crystallization or liquid crystalline ordering were also highlighted. image
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页数:20
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