Controlled Anionic Graft Polymerization of Ethylene Oxide Directly from Poly(N-isopropylacrylamide)

被引:36
|
作者
Zhao, Junpeng [1 ]
Schlaad, Helmut [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
关键词
OLIGO(ETHYLENE GLYCOL) METHACRYLATE; TRANSFER RADICAL POLYMERIZATION; CHAIN-TRANSFER POLYMERIZATION; RING-OPENING POLYMERIZATION; POLY(ETHYLENE OXIDE); BLOCK-COPOLYMERS; BRUSH COPOLYMERS; N-ISOPROPYLACRYLAMIDE; AQUEOUS-MEDIA; SIDE-CHAINS;
D O I
10.1021/ma2012392
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 study was conducted to demonstrate controlled anionic graft polymerization of ethylene oxide (EO) directly from poly(n-isopropylacrylamide) (PNIPAM). PNIPAM having an apparent number-averagemolecular weight of 43 kg/mol and a polydispersity index (PDI) of 1.13, as determined by size-exclusion chromatography (SEC), was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization. It was prepared using 3- benzylsulfanylthiocarbonylsulfanylpropionic acid (BPATT) as the chain transfer agent. The reactor was sealed by a stopcock and polymerization was conducted at 45 °C for 48 hours after the cryo-condensation of a predetermined amount of EO. Acetone, tetrahydrofuran (THF), and diethyl ether were used as received for RAFT polymerization and end-group removal, while THF was dried successively by Na and Na/K alloy for anionic graft polymerization. Acetone was evaporated and the residual solution of PNIPAM was dialyzed in cellulose membrane against distilled water for 3 days after quenching with rapid cooling.
引用
收藏
页码:5861 / 5864
页数:4
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