Amphiphilic fluorous random copolymer self-assembly for encapsulation of a fluorinated agrochemical

被引:16
|
作者
Ko, Jeong Hoon [1 ,2 ]
Bhattacharya, Arvind [1 ,2 ]
Terashima, Takaya [3 ]
Sawamoto, Mitsuo [3 ,4 ]
Maynard, Heather D. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, 607 Charles E Young Dr East, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif NanoSyst Inst, 607 Charles E Young Dr East, Los Angeles, CA 90095 USA
[3] Kyoto Univ, Dept Polymer Chem, Grad Sch Engn, Nishikyo Ku, Kyoto 6158510, Japan
[4] Chubu Univ, Inst Sci & Technol Res, 1200 Matsumoto Cho, Kasugai, Aichi 4878501, Japan
基金
日本学术振兴会; 美国国家科学基金会;
关键词
agrochemicals; amphiphilic polymer; fluorinated; polymer; fluorine; living radical polymerization; sugar; trehalose; CROSS-LINKING; TREHALOSE GLYCOPOLYMERS; STAR POLYMERS; STABILIZATION; STABILITY;
D O I
10.1002/pola.29187
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic self-folding random copolymers exhibit different solution behaviors depending on the identity of the hydrophobic/hydrophilic units. Herein, it is demonstrated that changing the hydrophilic unit from poly(ethylene glycol) to the sugar trehalose causes increased discrepancy in the polarity difference with a fluorinated hydrophobic segment and changes the aggregation state of the polymer in water. The PEG-fluorinated and trehalose/PEG-fluorinated amphiphilic random copolymers were the most efficient at encapsulating a fluorinated agrochemical. The small-molecule agrochemical exerts a strong influence on the self-assembly of the polymers, demonstrating that fluorous interactions result in not only intramolecular self-folding behavior but also intermolecular polymer association to form well-defined nanoparticles. (c) 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 352-359
引用
收藏
页码:352 / 359
页数:8
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