Development of a new class of rate-accelerating additives for nitroxide-mediated 'living' free radical polymerization

被引:102
作者
Malmstrom, E [1 ]
Miller, RD [1 ]
Hawker, CJ [1 ]
机构
[1] IBM CORP,ALMADEN RES CTR,CTR POLYMER INTERFACES & MACROMOL ASSEMBLIES,SAN JOSE,CA 95120
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0040-4020(97)00959-9
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Acylating agents have been identified as a new class of rate accelerating additives for nitroxide-mediated 'living' free radical polymerization. It is found that addition of 1 weight percent of acetic anhydride results in a significant decrease in the reaction time, 48 to 4 hours. This decrease in reaction time leads to greater control over the polymerization process with low polydispersity materials being obtained up to 150 000 a.m.u. A possible explanation for this effect is acylation of the alkoxyamine nitrogen leading to an increase in the lability of the C-ON bond. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:15225 / 15236
页数:12
相关论文
共 48 条
[1]   LIVING RADICAL POLYMERIZATION - KINETIC RESULTS [J].
CATALA, JM ;
BUBEL, F ;
HAMMOUCH, SO .
MACROMOLECULES, 1995, 28 (24) :8441-8443
[2]   Photochemical synthesis of TEMPO-capped initiators for ''living'' free radical polymerization [J].
Connolly, TJ ;
Baldovi, MV ;
Mohtat, N ;
Scaiano, JC .
TETRAHEDRON LETTERS, 1996, 37 (28) :4919-4922
[3]   Reactions of the ''stable'' nitroxide radical TEMPO. Relevance to ''living'' free radical polymerizations and autopolymerization of styrene [J].
Connolly, TJ ;
Scaiano, JC .
TETRAHEDRON LETTERS, 1997, 38 (07) :1133-1136
[4]  
DESAI A, 1997, POLYM MAT SCI ENG, V76, P152
[5]   ''Living'' free-radical polymerizations in the absence of initiators: Controlled autopolymerization [J].
Devonport, W ;
Michalak, L ;
Malmstrom, E ;
Mate, M ;
Kurdi, B ;
Hawker, CJ ;
Barclay, GG ;
Sinta, R .
MACROMOLECULES, 1997, 30 (07) :1929-1934
[6]   Polymer mobility in thin films [J].
Frank, B ;
Gast, AP ;
Russell, TP ;
Brown, HR ;
Hawker, CJ .
MACROMOLECULES, 1996, 29 (20) :6531-6534
[7]   FUNCTIONAL POLYMERS AND DENDRIMERS - REACTIVITY, MOLECULAR ARCHITECTURE, AND INTERFACIAL ENERGY [J].
FRECHET, JMJ .
SCIENCE, 1994, 263 (5154) :1710-1715
[8]   Well-defined block copolymers comprising styrene acrylonitrile random copolymer sequences synthesized by ''living'' radical polymerization [J].
Fukuda, T ;
Terauchi, T ;
Goto, A ;
Tsujii, Y ;
Miyamoto, T .
MACROMOLECULES, 1996, 29 (08) :3050-3052
[9]   MULTIFUNCTIONAL COUPLING AGENTS FOR LIVING CATIONIC POLYMERIZATION .2. BIFUNCTIONAL SILYL ENOL ETHERS FOR LIVING POLY(VINYL ETHERS) [J].
FUKUI, H ;
SAWAMOTO, M ;
HIGASHIMURA, T .
MACROMOLECULES, 1993, 26 (26) :7315-7321
[10]   CONTROLLED RADICAL POLYMERIZATION [J].
GAYNOR, S ;
GRESZTA, D ;
MARDARE, D ;
TEODORESCU, M ;
MATYJASZEWSKI, K .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 1994, A31 (11) :1561-1578