Synthesis and self-assembly of poly(styrene)-b-poly (N-vinylpyrrolidone) amphiphilic diblock copolymers made via a combined ATRP and MADIX approach

被引:50
作者
Hussain, H. [1 ]
Tan, B. H. [1 ]
Gudipati, C. S. [1 ]
Liu, Y. [1 ]
He, C. B. [1 ]
Davis, T. P. [1 ,2 ]
机构
[1] ASTAR, IMRE, Singapore 117602, Singapore
[2] Univ New S Wales, Sch Chem Sci & Engn, CAMD, Sydney, NSW 2052, Australia
关键词
atom transfer radical polymerization (ATRP); block copolymers; macromolecular design via the interchange of xanthates (MADIX); poly(N-vinylpyrrolidone); self-assembly;
D O I
10.1002/pola.22882
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 diblock copolymers of polystyrene (PS) and poly(N-vinylpyrrolidone) (PNVP) were prepared by a combination of ATRP and MADIX. Well-defined PS with bromine end group was synthesized by ATRP in bulk at 110 degrees C using (1-bromoethyl) benzene as an initiator. The Br- end group was then converted to xanthate as verified by H-1 NMR spectroscopy, elemental analysis, and UV-spectroscopy. PS-b-PNVP copolymers were produced by MADIX of NVP in bulk at 60 degrees C using PS-xanthate as a macro-chain transfer agent and the kinetics of polymerization were investigated. The structures of PS-b-PNVP were characterized using GPC and H-1 NMR. Amphiphilic PS-b-PNVP could form spherical micelles with PS cores and PNVP shells in aqueous solution as confirmed by H-1 NMR and laser light scattering (LLS). The values of critical micelle concentration of PS-b-PNVP and the average aggregation number of PS-b-PNVP in the micelles were measured using pyrene as a probe and static LLS, respectively. The aggregation number increases concomitantly with temperature (10-50 degrees C), but the hydrodynamic radius of the micelles remains almost constant over the same temperature range, which may indicate shell dehydration at a higher temperature. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:5604 / 5615
页数:12
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