ABx-type amphiphilic macromonomer-based supramolecular hyperbranched polymers for controllable self-assembly

被引:24
|
作者
Liu, Tingting
Wang, Shuodong
Song, Yanli
Li, Jiawei
Yan, Hongxia
Tian, Wei [1 ]
机构
[1] Northwestern Polytech Univ, Key Lab Space Appl Phys & Chem, Minist Educ, Xian 710072, Peoples R China
基金
美国国家科学基金会;
关键词
HOST-GUEST INTERACTIONS; LARGE MULTIMOLECULAR MICELLES; MOLECULAR RECOGNITION; METAL-COORDINATION; POLYMERIZATION; COPOLYMERS; VESICLES; COMPLEX; SCATTERING; BEHAVIORS;
D O I
10.1039/c6py02215d
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A macromonomer strategy has displayed potential advantages of constructing functional supramolecular hyperbranched polymers (SHPs); however, owing to the limited functional group number and weak noncovalent interactions, it is difficult to control the dynamic self-assembly process of SHPs based on the reported AB(2)-type hydrophilic macromonomers. In this work, a novel SHP was first constructed using an AB(x)-type (x > 2) amphiphilic macromonomer for tuning its self- assembly morphology, size and dynamic process. The obtained SHPs formed ellipsoidal unimolecular micelles with sizes of approximately 10 nm by directly dissolving SHP precursors in a 0.5 mol L-1 NaCl solution. These unimolecular micelles further self- assembled into branched aggregates in aqueous solutions after the removal of NaCl. SHP- based unimolecular micelles present a higher sensitivity for drug sensing in comparison with further branched self-assemblies. Obtaining SHPs through the AB(x)-type amphiphilic macromonomer may be a novel strategy to deeply investigate the relationships between polymer structures and self- assemblies and regulate their functionality.
引用
收藏
页码:1306 / 1314
页数:9
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