Uni-molecular nanoparticles of poly(2-oxazoline) showing tunable thermoresponsive behaviors

被引:12
作者
Chu, Yuehuan [1 ]
Li, Huaan [1 ]
Huang, Huahua [1 ]
Zhou, Houbo [1 ]
Chen, Yi [1 ]
Andreas, Bockler [1 ]
Liu, Lixin [1 ]
Chen, Yongming [1 ]
机构
[1] Sun Yat Sen Univ, Minist Educ, Key Lab Polymer Composite & Funct Mat, Sch Mat Sci & Engn, 135 Xingang Xi Rd, Guangzhou 510275, Guangdong, Peoples R China
关键词
grafting-onto method; poly(2-oxazoline); polymer brush; thermoresponsive polymers; CRITICAL SOLUTION TEMPERATURE; HIGHLY EFFICIENT SYNTHESIS; POLYMER BRUSHES; SIDE-CHAINS; AQUEOUS-SOLUTION; COMB; POLY(2-ETHYL-2-OXAZOLINE); COPOLYMERIZATION; NANOOBJECTS; SURFACES;
D O I
10.1002/pola.28889
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Herein, cylindrical molecular bottlebrushes grafted with poly(2-oxazoline) (POx) as a shaped tunable uni-molecular nanoparticle were synthesized via the grafting-onto approach. First, poly(glycidyl methacrylate) (PGMA) backbones with azide pendant units were prepared via reversible addition fragmentation transfer (RAFT) polymerization followed by post-modification. The degree of polymerization (DP) of the backbones was tuned in a range from 20 to 800. Alkynyl-terminated POx side chains were synthesized by living cationic ring opening polymerization (LCROP) of 2-ethyl-2-oxazoline (EtOx) and 2-methyl-2-oxazoline (MeOx), respectively. The DP of side chains was varied between 20 and 100. Then, the copper-catalyzed azide-alkynyl cycloaddition (CuAAC) click chemistry was conducted with a feed ratio of [alkynyl]:[azide]=1.2:1 to yield a series of brushes. Depending on the DP of side chains, the grafting density ranged between 47 and 85%. The resulting brushlike nanoparticles exhibited shapes of sphere, rod and worm. Aqueous solutions of PEtOx brushes demonstrated a thermoresponsive behavior as a function of the length of backbones and side chains. Surprisingly, it was found that the lower critical solution temperature of PEtOx brushes increased with a length increase of backbones. (c) 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 174-183
引用
收藏
页码:174 / 183
页数:10
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