Surface-Dependent Kinetics of Cu(0)-Wire-Catalyzed Single-Electron Transfer Living Radical Polymerization of Methyl Acrylate in DMSO at 25 °C

被引:239
作者
Nguyen, Nga H. [1 ]
Rosen, Brad M. [1 ]
Lligadas, Gerard [1 ]
Percec, Virgil [1 ]
机构
[1] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
SET-LRP; DENDRITIC MACROMOLECULES; CONVENTIONAL MONOMERS; DIVERGENT SYNTHESIS; ITERATIVE STRATEGY; CATALYTIC-ACTIVITY; COPPER; METHACRYLATE; COMBINATION; POLYACRYLATES;
D O I
10.1021/ma8028562
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The effect of Cu(0) wire dimensions Oil the Cu(0) wire/Me-6-TREN-catalyzed heterogeneous single-electron transfer living radical polymerization (SET-LRP) of methyl acrylate (MA) initiated with methyl 2-bromopropionate (MBP) in DMSO at 25 degrees C was analyzed by kinetic experiments. These kinetic results were compared with those of Cu(0) powder/Me-6-TREN-catalyzed SET-LRP. Both wire and powder produce perfect SET-LRP with a first-order rate of polymerization in growing species Lip to 100% conversion. Nevertheless, Cu(0) wire experiments demonstrated SET-LRP with greater perfection, allowing for the accurate determination of the external rate order (vis-a-vis Surface area) for heterogeneous Cu(0) catalyst and accurate prediction of k(p)(app) from wire dimension. Cu(0) wire also exhibited a significantly greater control of molecular weight distribution than Cu(0) powder. The combined advantages of easier catalyst preparation, handling, predictability, tunability, simple recovery/recycling, and enhanced control of molecular weight distribution make Cu(0)-wire-catalyzed SET-LRP the ideal methodology for the synthesis of tailored polyacrylates.
引用
收藏
页码:2379 / 2386
页数:8
相关论文
共 55 条
[1]  
BAKERJIAN R, 1988, TOOL MANUFACTURING E
[2]   Outer-sphere electron transfer metal-catalyzed polymerization of styrene using a macrobicyclic ligand [J].
Bell, Craig A. ;
Whittaker, Michael R. ;
Gahan, Lawrence R. ;
Monteiro, Michael J. .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (01) :146-154
[3]   5-COORDINATED HIGH-SPIN COMPLEXES OF BIVALENT COBALT NICKEL AND COPPER WITH TRIS(2-DIMETHYLAMINOETHYL)AMINE [J].
CIAMPOLINI, M ;
NARDI, N .
INORGANIC CHEMISTRY, 1966, 5 (01) :41-+
[4]   Kinetics and mechanism of reaction of carbon tetrachloride with copper(0) in dimethylformamide [J].
Egorov, AM ;
Matyukhova, SA ;
Anisimov, AV .
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2005, 75 (07) :1131-1135
[5]   Kinetics and mechanism of the reaction of benzyl bromide with copper in hexamethylphosphoramide [J].
Egorov, AM ;
Matyukhova, SA ;
Anisimov, AV .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2005, 37 (05) :296-305
[6]   Kinetics of reaction of copper with substituted benzyl chlorides in dipolar aprotic solvents [J].
Egorov, Anatoly M. ;
Matyukhova, Svetlana A. .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2007, 39 (10) :547-555
[7]   The persistent radical effect: A principle for selective radical reactions and living radical polymerizations [J].
Fischer, H .
CHEMICAL REVIEWS, 2001, 101 (12) :3581-3610
[8]  
Fischer H, 1999, J POLYM SCI POL CHEM, V37, P1885, DOI 10.1002/(SICI)1099-0518(19990701)37:13<1885::AID-POLA1>3.3.CO
[9]  
2-T
[10]   Chemistry - Precious little catalyst [J].
Goodman, D. Wayne .
NATURE, 2008, 454 (7207) :948-949