Highly Efficient Synthesis of Low Polydispersity Core Cross-Linked Star Polymers by Ru-Catalyzed Living Radical Polymerization

被引:21
作者
Goh, Tor Kit [2 ]
Yamashita, Satoshi [1 ]
Satoh, Kotaro [1 ]
Blencowe, Anton [2 ]
Kamigaito, Masami [1 ]
Qiao, Greg G. [2 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 4648603, Japan
[2] Univ Melbourne, Dept Chem & Biomol Engn, Polymer Sci Grp, Melbourne, Vic 3010, Australia
基金
澳大利亚研究理事会; 日本学术振兴会;
关键词
atom transfer radical polymerization; catalysts; living polymerization; microgels; star polymers; CATIONIC-POLYMERIZATION; METHYL-METHACRYLATE; HONEYCOMB FILMS; MICROGEL CORES; COPOLYMERS; COMPLEXES; COATINGS; DESIGN;
D O I
10.1002/marc.201000641
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 efficient formation of low polydispersity core cross-linked star (CCS) polymers via controlled/living radical polymerization (LRP) and the arm-first approach was found to be dependant on the mediating catalyst system. The Ru catalyst, Ru(Ind)Cl(PPh3)(2) Cat. 1, and tertiary amine co-catalyst were used to synthesize highly living poly(methyl methacrylate) (PMMA) macroinitiators, which were then linked together with ethylene glycol dimethacrylate (EGDMA) to form PMMA(arm)-PEGDMA(core) CCS polymers. The quantitative and near-quantitative synthesis of CCS polymers were observed for low to moderate molecular weight macroinitiators ((M) over bar (n) = 8 and 20 kDa), respectively. Lower conversions were observed for high-molecular weight macroinitiators ((M) over bar (n) >= 60 kDa). Overall, an improvement of between 10 and 20% was observed when comparing the Cat. 1 system to a conventional Cu-catalyzed system. This significant improvement in macroinitiator-to-star conversion is explained in the context of catalyst system selection and CCS polymer formation.
引用
收藏
页码:456 / 461
页数:6
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