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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.
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页码:456 / 461
页数:6
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