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Ionic liquid-mediated synthesis and self-assembly of poly(ethylene glycol)-block-polystyrene copolymer by ATRP method
被引:10
作者:
Van Hoa Nguyen
[1
,2
]
Shim, Jae-Jin
[1
]
机构:
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 712749, Gyeongbuk, South Korea
[2] Nha Trang Univ, Dept Chem, Nha Trang, Vietnam
基金:
新加坡国家研究基金会;
关键词:
Block copolymer;
Ionic liquid;
Self-assembly;
ATRP polymerization;
TRANSFER RADICAL POLYMERIZATION;
AMPHIPHILIC BLOCK-COPOLYMERS;
METHACRYLATE;
OXIDE);
DIBLOCK;
STYRENE;
MORPHOLOGIES;
BEHAVIOR;
D O I:
10.1007/s00396-014-3431-5
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Poly(ethylene glycol)-block-polystyrene (PEG-b-PS) was synthesized by the atom transfer radical polymerization of styrene using PEG-Br as the macroinitiator in an ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]). CuBr and 2,2aEuro(3)-bipyridyl were used as the catalyst and ligand, respectively. The structure, composition, and molecular weight of the PEG-b-PS copolymer were characterized by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance, and gel permeation chromatography. The PEG-b-PS copolymer with a high molecular weight (M (n) = 51,000 g mol(-1)) and relatively low polydispersity index (PDI = 1.35) was formed at 110 A degrees C for 5 h. Self-assembly of this amphiphilic block copolymer in toluene at different concentrations and in dimethylformamide (DMF)/water systems was also examined. Transmission electron microscopy showed that the block copolymer formed different morphologies spontaneously according to the different solvent systems used.
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页码:617 / 623
页数:7
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