Copper(0)-Mediated Living Radical Polymerization of Acrylonitrile: SET-LRP or AGET-ATRP

被引:50
作者
Liu, Xiao-Hui [1 ]
Zhang, Gui-Bao [1 ]
Li, Bai-Xiang [1 ]
Bai, Yun-Gang [1 ]
Li, Yue-Sheng [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
acrylonitrile; living polymerization; living radical polymerization; molar mass distribution; molecular weight distribution; radical polymerization; UV-vis spectroscopy; FRAGMENTATION CHAIN TRANSFER; HIGHER-MOLECULAR-WEIGHT; ELECTRON-TRANSFER; METHYL ACRYLATE; 25-DEGREES-C; KINETICS; COPOLYMERS; POLYMERS; DMSO;
D O I
10.1002/pola.24350
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cu(0)-mediated living radical polymerization was first extended to acrylonitrile (AN) to synthesize polyacrylonitrile with a high molecular weight and a low polydispersity index. This was achieved by using Cu(0)/hexamethylated tris(2-amino-ethyl)amine (Me(6)-TREN) as the catalyst, 2-bromopropionitrile as the initiator, and dimethyl sulfoxide (DMSO) as the solvent. The reaction was performed under mild reaction conditions at ambient temperature and thus biradical termination reaction was low. The rapid and extensive disproportionation of Cu(I)Br/Me(6)-TREN in DMSO/AN supports a mechanism consistent with a single electron transfer-living radical polymerization (SET-LRP) rather than activators generated by electron transfer atom transfer radical polymerization (AGET ATRP). (1)H NMR analysis and chain extension experiment confirm the high chain-end functionality of the resultant polymer. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 5439-5445, 2010
引用
收藏
页码:5439 / 5445
页数:7
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