ICAR ATRP with ppm Cu Catalyst in Water

被引:226
作者
Konkolewicz, Dominik [1 ]
Magenau, Andrew J. D. [1 ]
Averick, Saadyah E. [1 ]
Simakova, Antonina [1 ]
He, Hongkun [1 ]
Matyjaszewski, Krzysztof [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Ctr Macromol Engn, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
TRANSFER RADICAL POLYMERIZATION; FRAGMENTATION CHAIN TRANSFER; CONDENSING VINYL POLYMERIZATION; ELECTRON-TRANSFER; HYPERBRANCHED POLYACRYLATES; AQUEOUS-MEDIA; METHACRYLATE; COPOLYMERS; PROTEIN; (METH)ACRYLATES;
D O I
10.1021/ma300887r
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Initiators for continuous activator regeneration atom transfer radical polymerization (ICAR ATRP) with ppm amount of Cu catalyst was successfully developed in water. For the first time, Cu catalyst concentrations of 100 ppm and lower were used in aqueous media to prepare well-defined macromolecules. Polymers of oligo(ethylene oxide) methyl ether acrylate were synthesized with low dispersity (M-w/M-n = 1.15-1.28) using 20-100 ppm of an active CuBr/tris(pyridin-2-ylrnethyl)amine-based catalyst in the presence of excess bromide anions. This technique was used to synthesize a thermoresponsive block copolymer of poly(oligo(ethylene oxide) methyl ether methacrylate)-b-poly(oligo(ethylene oxide) methyl ether acrylate). The methacrylic block had a lower critical solution temperature (LCST = 77 +/- 2 degrees C) below that of the acrylic block. The hydrodynamic diameter of ca. 10 nm at temperatures below the LCST is consistent with free polymer chains in solution, and the diameter of ca. 30 nm above the LCST is consistent with a micellar structure. The aqueous ICAR ATRP technique was also used to successfully synthesize a well-defined bioconjugate by growing poly(oligo(ethylene oxide) acrylate) from a bovine serum albumin (BSA) protein functionalized with ca. 30 ATRP initiating sites.
引用
收藏
页码:4461 / 4468
页数:8
相关论文
共 78 条
[1]   First example of the atom transfer radical polymerisation of an acidic monomer: direct synthesis of methacrylic acid copolymers in aqueous media [J].
Ashford, EJ ;
Naldi, V ;
O'Dell, R ;
Billingham, NC ;
Armes, SP .
CHEMICAL COMMUNICATIONS, 1999, (14) :1285-1286
[2]   ATRP under Biologically Relevant Conditions: Grafting from a Protein [J].
Averick, Saadyah ;
Simakova, Antonina ;
Park, Sangwoo ;
Konkolewicz, Dominik ;
Magenau, Andrew J. D. ;
Mehl, Ryan A. ;
Matyjaszewski, Krzysztof .
ACS MACRO LETTERS, 2012, 1 (01) :6-10
[3]   The future of reversible addition fragmentation chain transfer polymerization [J].
Barner-Kowollik, Christopher ;
Perrier, Sebastien .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (17) :5715-5723
[4]   Streptavidin as a macroinitiator for polymerization: In situ protein-polymer conjugate formation [J].
Bontempo, D ;
Maynard, HD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (18) :6508-6509
[5]   Controlled Aqueous Atom Transfer Radical Polymerization with Electrochemical Generation of the Active Catalyst [J].
Bortolamei, Nicola ;
Isse, Abdirisak A. ;
Magenau, Andrew J. D. ;
Gennaro, Armando ;
Matyjaszewski, Krzysztof .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (48) :11391-11394
[6]   Controlled/living radical polymerization: Features, developments, and perspectives [J].
Braunecker, Wade A. ;
Matyjaszewski, Krzysztof .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (01) :93-146
[7]   Thermodynamic Components of the Atom Transfer Radical Polymerization Equilibrium: Quantifying Solvent Effects [J].
Braunecker, Wade A. ;
Tsarevsky, Nicolay V. ;
Gennaro, Armando ;
Matyjaszewski, Krzysztof .
MACROMOLECULES, 2009, 42 (17) :6348-6360
[8]   Living free-radical polymerization by reversible addition-fragmentation chain transfer: The RAFT process [J].
Chiefari, J ;
Chong, YK ;
Ercole, F ;
Krstina, J ;
Jeffery, J ;
Le, TPT ;
Mayadunne, RTA ;
Meijs, GF ;
Moad, CL ;
Moad, G ;
Rizzardo, E ;
Thang, SH .
MACROMOLECULES, 1998, 31 (16) :5559-5562
[9]  
Coca S, 1998, J POLYM SCI POL CHEM, V36, P1417, DOI 10.1002/(SICI)1099-0518(19980715)36:9<1417::AID-POLA9>3.0.CO
[10]  
2-P