Soluble and recoverable support for copper bromide-mediated living radical polymerizatian

被引:65
作者
Shen, YQ [1 ]
Zhu, SP [1 ]
Pelton, R [1 ]
机构
[1] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L7, Canada
关键词
D O I
10.1021/ma001948g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Transition-metal-mediated living radical polymerizations (atom transfer radical polymerization, ATRP) have many potential applications, but the high concentration of residual catalyst colors their products. Supporting catalyst on insoluble solids has been used to reduce the content of residual catalyst and to reuse the catalyst, but the ability of the supported catalyst to mediate a polymerization is substantially reduced due to heterogeneity. Here we report a soluble but recoverable catalyst support for ATRP. Polg(ethylene)-block-poly(ethylene glycol) (PE-PEG) was soluble in toluene above 70 degreesC but insoluble at room temperature. CuBr supported on PE-PEG via tetraethyldiethylenetriamine thus mediated Living polymerizations of methyl methacrylate, 2-(dimethylamino)ethyl methacrylate, and styrene as homogeneous catalyst at 80 or 100 degreesC, producing polymers with well-controlled molecular weight and very low polydispersity. The catalyst recycled at ambient temperature retained high activity and still mediated living polymerizations as well as the fresh catalyst. Subsequent block copolymerization confirmed its living nature.
引用
收藏
页码:3182 / 3185
页数:4
相关论文
共 26 条
[1]   Thermoresponsive polymer-bound substrates [J].
Bergbreiter, DE ;
Caraway, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (25) :6092-6093
[2]   SMART LIGANDS THAT REGULATE HOMOGENEOUSLY CATALYZED-REACTIONS [J].
BERGBREITER, DE ;
ZHANG, L ;
MARIAGNANAM, VM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (20) :9295-9296
[3]   POLYETHYLENE-BOUND SOLUBLE RECOVERABLE PALLADIUM(0) CATALYSTS [J].
BERGBREITER, DE ;
WEATHERFORD, DA .
JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (11) :2726-2730
[4]   The use of soluble polymers to effect homogeneous catalyst separation and reuse [J].
Bergbreiter, DE .
CATALYSIS TODAY, 1998, 42 (04) :389-397
[5]  
HADDLETON DM, 1999, CHEM COMMUN, V99
[6]   Controlled synthesis of polymer brushes by "Living" free radical polymerization techniques [J].
Husseman, M ;
Malmström, EE ;
McNamara, M ;
Mate, M ;
Mecerreyes, D ;
Benoit, DG ;
Hedrick, JL ;
Mansky, P ;
Huang, E ;
Russell, TP ;
Hawker, CJ .
MACROMOLECULES, 1999, 32 (05) :1424-1431
[7]   The effect of molecular architecture on the thermotropic behavior of poly[11-(4′-cyanophenyl-4"-phenoxy)undecyl acrylate] and its relation to polydispersity [J].
Kasko, AM ;
Heintz, AM ;
Pugh, C .
MACROMOLECULES, 1998, 31 (02) :256-271
[8]   POLYMERIZATION OF METHYL-METHACRYLATE WITH THE CARBON-TETRACHLORIDE DICHLOROTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM(II) METHYLALUMINUM BIS(2,6-DI-TERT-BUTYLPHENOXIDE) INITIATING SYSTEM - POSSIBILITY OF LIVING RADICAL POLYMERIZATION [J].
KATO, M ;
KAMIGAITO, M ;
SAWAMOTO, M ;
HIGASHIMURA, T .
MACROMOLECULES, 1995, 28 (05) :1721-1723
[9]   Immobilization of the copper catalyst in atom transfer radical polymerization [J].
Kickelbick, G ;
Paik, HJ ;
Matyjaszewski, K .
MACROMOLECULES, 1999, 32 (09) :2941-2947
[10]   Controlled radical polymerization of methyl methacrylate in the presence of palladium acetate, triphenylphosphine, and carbon tetrachloride [J].
Lecomte, P ;
Drapier, I ;
Dubois, P ;
Teyssie, P ;
Jerome, R .
MACROMOLECULES, 1997, 30 (24) :7631-7633