Reversible addition-fragmentation chain-transfer graft polymerization of styrene: Solid phases for organic and peptide synthesis

被引:105
作者
Barner, L
Zwaneveld, N
Perera, S
Pham, Y
Davis, TP [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn & Ind Chem, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
[2] Mimotopes Proprietary Ltd, Clayton, Vic 3168, Australia
关键词
living polymerization; radiation; reversible addition-fragmentation chain transfer (RAFT); graft copolymers; solid phase surfaces for combinatorial chemistry;
D O I
10.1002/pola.10513
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
The gamma-initiated reversible addition-fragmentation chain-transfer (RAFT)agent-mediated free-radical graft polymerization of styrene onto a polypropylene solid phase has been performed with cumyl phenyldithioacetate (CPDA). The initial CPDA concentrations range between 1 x 10(-2) and 2 x 10(-3) mol L-1 with dose rates of 0.18, 0.08, 0.07, 0.05, and 0.03 kGy h(-1). The RAFT graft polymerization is compared with the conventional free-radical graft polymerization of styrene onto polypropylene. Both processes show two distinct regimes of grafting: (1) the grafting layer regime, in which the surface is not yet totally covered with polymer chains, and (2) a regime in which a second polymer layer is formed. Here, we hypothesize that the surface is totally covered with polymer chains and that new polymer chains are started by polystyrene radicals from already grafted chains. The grafting ratio of the RAFT-agent-mediated process is controlled via the initial CPDA concentration. The molecular weight of the polystyrene from the solution (PSfree) shows a linear behavior with conversion and has a low polydispersity index. Furthermore, the loading of the grafted solid phase shows a linear relationship with the molecular weight of PSfree for both regimes. Regime 2 has a higher loading capacity per molecular weight than regime 1. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:4180 / 4192
页数:13
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