Macromolecular architectural effects on solution self-assembly of amphiphilic AB-type block copolymers

被引:7
|
作者
Ozawa, Naoki [1 ]
Nishimura, Tomoki [1 ]
机构
[1] Shinshu Univ, Dept Chem & Mat Sci, 3-15-1 Tokida, Ueda, Nagano 3868567, Japan
基金
日本学术振兴会;
关键词
RING-OPENING POLYMERIZATION; EXPANSION METATHESIS POLYMERIZATION; CYCLIC DIBLOCK COPOLYMERS; MIKTOARM STAR COPOLYMERS; TRIBLOCK COPOLYMERS; MICELLAR PROPERTIES; PHASE-TRANSITION; ETHYLENE-OXIDE; THERMORESPONSIVE BEHAVIOR; MOLECULAR ARCHITECTURE;
D O I
10.1039/d3py01324c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymers with different architectures, such as block, graft, star, and cyclic polymers, have been developed owing to recent advances in synthetic technology. Notably, minor changes in the architecture of amphiphilic polymers can lead to different self-assembly behaviors, even when their molecular weights and hydrophilic-hydrophobic compositions are similar. This variation in the self-assembly behavior directly affects the properties and performance of self-assembled polymer-based materials. However, a clear understanding of how changes in polymer architecture influence self-assembly behavior is still emerging. This review aims to compare the self-assembly behaviors of amphiphilic AB-type block copolymers with different molecular architectures and elucidate how different polymer architectures influence self-assembly behaviors, as well as their underlying mechanisms. The discussion extends to recent applications, demonstrating how changes in polymer architecture can influence the performance of polymer assemblies used as carriers in drug delivery systems. This review discusses the self-assembly of amphiphilic linear and various non-linear polymers such as star and cyclic architectures, highlighting how polymer architecture impacts self-assembly behavior.
引用
收藏
页码:349 / 370
页数:22
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