Synthesis of cyclic amphiphilic homopolymers and their potential application as polymeric micelles

被引:39
|
作者
Laurent, Boyd A. [1 ]
Grayson, Scott M. [1 ]
机构
[1] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
基金
美国国家科学基金会;
关键词
FRAGMENTATION CHAIN TRANSFER; BLOCK-COPOLYMER MICELLES; CROSS-LINKED KNEDELS; CLICK CHEMISTRY; UNIMOLECULAR MICELLES; AQUEOUS-SOLUTION; STAR POLYMERS; CONJUGATED POLYMERS; DIBLOCK COPOLYMERS; PHASE-TRANSITION;
D O I
10.1039/c1py00378j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Although amphiphilic copolymers have been widely studied due to their ability to phase segregate in bulk and form micelle-like nanostructures in solution, previous research has focused primarily on block copolymers. Amphiphilic homopolymers, in which each monomer along the backbone contains an amphiphilic unit, have seen only limited exploration, while non-linear amphiphilic homopolymers remain largely unexplored. Building from methods established in our laboratories for the synthesis of cyclic polymers, bifurcated amphiphiles were attached via a highly efficient "click" coupling to access analogous sets of linear and cyclic amphiphilic homopolymers (the first reported example of cyclic amphiphilic homopolymers). These amphiphilic homopolymers showed solubility in a wide range of solvents with varying polarities and also have demonstrated the ability to encapsulate guests in incompatible solvents. For the mass range examined, the cyclic polymers showed only a negligible difference in guest encapsulation when compared to linear analogs.
引用
收藏
页码:1846 / 1855
页数:10
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