Synthesis and properties of polydimethylsiloxane-containing block copolymers via living radical polymerization

被引:83
作者
Huan, K
Bes, L
Haddleton, DM [1 ]
Khoshdel, E
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[2] Unilever Res, Wirral CH63 3JW, Merseyside, England
关键词
block copolymer; amphiphilic; siloxane; living radical polymerization; copper;
D O I
10.1002/pola.1161
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polydimethylsiloxane (PDMS) block copolymers were synthesized by using PDMS macroinitiators with copper-mediated living radical polymerization. Diamino PDMS led to initiators that gac-e ABA block copolymers, but there was low initiator efffciency and molecular weights are somewhat uncontrolled. The use of mono- and difunctional carbinol-hydroxyl functional initiators led to AB and ABA block copolymers with nar row polydispersity indices (PDIs) and controlled number-average molecular weights (M-n's). Polymerization with methyl methacrylate (MMA) and X-dimethyl aminoethyl methacrylate (DMAEMA) was discovered with a range of molecular weights produced. Polymerizations proceeded with excellent first-order kinetics indicative of living polymerization. ABA block copolymers with MMA were prepared with between 28 and 84 wt % poly(methyl methacrylate) with M-n's between 7.6 and 35 K (PDI <1.30), which show thermal transitions characteristic of block copolymers: ABA block copolymers with DMAEMA led to amphiphilic block copolymers with M-n's between 9.5 and 4.5.7 K (PDIs of 1.25-1.70), which formed aggregates in solution with a critical micelle concentration of 0.1 g dm(-3) as determined by pyrene fluorimetry experiments. Monocarbinol functional PDMS gave AB block copolymers with both MMA and DMAEMA. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:1833 / 1842
页数:10
相关论文
共 24 条
[1]   Evidence for the low thermal stability of poly(methyl methacrylate) polymer produced by atom transfer radical polymerisation [J].
Borman, CD ;
Jackson, AT ;
Bunn, A ;
Cutter, AL ;
Irvine, DJ .
POLYMER, 2000, 41 (15) :6015-6020
[2]  
DEPAZBANEZ MV, 2000, MACROMOLECULES, V33, P451
[3]  
DOWSON D, 1974, ADV POLYM FRICTION B, V5, P533
[4]   Atom transfer radical polymerization of methyl methacrylate initiated by alkyl bromide and 2-pyridinecarbaldehyde imine copper(I) complexes [J].
Haddleton, DM ;
Jasieczek, CB ;
Hannon, MJ ;
Shooter, AJ .
MACROMOLECULES, 1997, 30 (07) :2190-2193
[5]   Phenolic ester-based initiators for transition metal mediated living polymerization [J].
Haddleton, DM ;
Waterson, C .
MACROMOLECULES, 1999, 32 (26) :8732-8739
[6]   Atom transfer radical polymerisation (ATRP) of methyl methacrylate in the presence of radical inhibitors [J].
Haddleton, DM ;
Clark, AJ ;
Crossman, MC ;
Duncalf, DJ ;
Heming, AM ;
Morsley, SR ;
Shooter, AJ .
CHEMICAL COMMUNICATIONS, 1997, (13) :1173-1174
[7]   Monohydroxy terminally functionalised poly(methyl methacrylate) from atom transfer radical polymerisation [J].
Haddleton, DM ;
Waterson, C ;
Derrick, PJ ;
Jasieczek, CB ;
Shooter, AJ .
CHEMICAL COMMUNICATIONS, 1997, (07) :683-684
[8]   Atom transfer polymerization of methyl methacrylate mediated by alkylpyridylmethanimine type ligands, copper(I) bromide, and alkyl halides in hydrocarbon solution [J].
Haddleton, DM ;
Crossman, MC ;
Dana, BH ;
Duncalf, DJ ;
Heming, AM ;
Kukulj, D ;
Shooter, AJ .
MACROMOLECULES, 1999, 32 (07) :2110-2119
[9]  
HADDLETON DM, 1997, J MACROMOLECULES, V31, P2016
[10]  
HATADA K, 1993, J PURE APPL CHEM, P645