Selective Encapsulation of Ionic Dyes by Core/Shell Amphiphilic Macromolecules Derived from Hyperbranched Polyethylenimine: Properties through Structures

被引:14
|
作者
Wan, Decheng [1 ]
Lai, Yi [1 ]
Jin, Ming [1 ]
Pu, Hongting [1 ,2 ]
机构
[1] Tongji Univ, Inst Funct Polymers, Sch Mat Sci & Engn, Shanghai 201804, Peoples R China
[2] Tongji Univ, Key Lab Adv Civil Engn Mat, Minist Educ, Shanghai 201804, Peoples R China
关键词
covalent micelles; host/guest systems; molecular recognition; separation; SUPRAMOLECULAR NANOCAPSULE; MOLECULAR NANOCAPSULES; BETA-CYCLODEXTRIN; RECOGNITION; POLYMER; ARCHITECTURES; COPOLYMERS; MECHANISM; MICELLES; BEHAVIOR;
D O I
10.1002/macp.201100186
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Reverse-micelle-like CAMs derived from HPEI, which exist as either aggregates or unimolecular micelles, show selectivity upon the encapsulation of water-soluble and ionic dyes. For rigid dyes, the encapsulating ability is very weak, while for less rigid ones, the encapsulation is dependent on their electronic properties. Through electronic engineering of the CAM, the complementary CAM/dye interaction strengths can be greatly favored or disfavored. Electronic engineering of the CAM can also exert a non-linear effect on the guest affinities and thus amplify the difference of the competitive guest species and further lead to highly selective encapsulations. Even if one dye species is complexed by another dye species, highly selective encapsulation can still be realized by a CAM.
引用
收藏
页码:1910 / 1917
页数:8
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