Synthesis of water-soluble cationic polymers with star-like structure based on cyclodextrin core via ATRP

被引:70
作者
Li, JS
Xiao, HN [1 ]
Kim, YS
Lowe, TL
机构
[1] Univ New Brunswick, Dept Chem Engn, Fredericton, NB E3B 5A3, Canada
[2] Penn State Univ, Dept Surg, Hershey, PA 17033 USA
[3] Penn State Univ, Dept Bioengn, Hershey, PA 17033 USA
[4] Penn State Univ, Dept Mat Sci & Engn, Hershey, PA 17033 USA
关键词
atom transfer radical polymerization (ATRP); colloidal titration; dynamic light scattering (DLS); star polymer; water-soluble polymer;
D O I
10.1002/pola.21058
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
A range of novel cationic star-like polymers (Star-P(MeDMA)s) were synthesized through atom transfer radical polymerization (ATRP) by core-first method, using a beta-cyclodextrin initiator with 21 initiation sites (21Br-beta-CD). Methyl chloride-quaternized 2-(dimethylamino)ethyl methacrylate (MeDMA) was polymerized in an aqueous medium using 21Br-beta-CD, Cu(I)Br, and 2,2'-dipyridyl as an initiator, catalyst, and ligand, respectively. The effects of polymerization temperature and monomer/initiator ratios on the degree and kinetics of polymerization were investigated. The molecular weights, hydrodynamic sizes, and charge densities of the quaternized polymers were characterized using gel permeation chromatography (GPC), dynamic light scattering (DLS), and colloidal titration, respectively. The results demonstrated that the moderate aqueous solubility of the 21Br-beta-CD initiator had significant impact on the physicochemical properties of the obtained star polymers. The polymerization of 500/1/2/5 ([M](0)/[I](0)/ [Cu(I)(0)/[L](0)]) at 90 degrees C for 6 h was found to be the best condition to synthesize the proposed cationic star polymer with well-defined structures in aqueous medium. The nonlinear relationship between the apparent charge density and the particle size of the cationic star polymers was further revealed by GPC and DLS measurements. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:6345 / 6354
页数:10
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