Dendrimers as scaffolds for multifunctional reversible addition-fragmentation chain transfer agents:: Syntheses and polymerization

被引:92
作者
Hao, XJ
Nilsson, C
Jesberger, M
Stenzel, MH
Malmström, E
Davis, TP
Östmark, E
Barner-Kowollik, C [1 ]
机构
[1] Univ New S Wales, Ctr Adv Macromol Design, Sch Chem Engn & Ind Chem, Sydney, NSW 2052, Australia
[2] Royal Inst Technol, SE-10044 Stockholm, Sweden
关键词
dendrimers; free-radical polymerization; kinetics (polym.); reversible addition fragmentation chain transfer (RAFT);
D O I
10.1002/pola.20434
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The synthesis and characterization of novel first- and second-generation true dendritic reversible addition-fragmentation chain transfer (RAFT) agents carrying 6 or 12 pendant 3-benzylsulfanylthiocarbonylsulfanylpropionic acid RAFT end groups with Z-group architecture based on 1,1,1-hydroxyphenyl ethane and trimethylolpropane cores are described in detail. The multifunctional dendritic RAFT agents have been used to prepare star polymers of poly(butyl acrylate) (PBA) and polystyrene (PS) of narrow polydispersities (1.4 < polydispersity index < 1.1 for PBA and 1.5 < polydispersity index < 1.3 for PS) via bulk free-radical polymerization at 60 degreesC. The novel dendrimer-based multifunctional RAFT agents effect an efficient living polymerization process, as evidenced by the linear evolution of the number-average molecular weight (M.) with the monomer-polymer conversion, yielding star polymers with molecular weights of up to M-n = 160,000 g mol(-1) for PBA (based on a linear PBA calibration) and up to M. = 70,000 g mol(-1) for PS (based on a linear PS calibration). A structural change in the chemical nature of the dendritic core (i.e., 1,1,1-hydroxyphenyl ethane vs trimethylolpropane) has no influence on the observed molecular weight distributions. The star-shaped structure of the generated polymers has been confirmed through the cleavage of the pendant arms off the core of the star-shaped polymeric materials. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:5877 / 5890
页数:14
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