Cooperative and Synergistic Solvent Effects in SET-LRP of MA

被引:133
作者
Jiang, Xuan [1 ]
Fleischmann, Sven [1 ]
Nguyen, Nga H. [1 ]
Rosen, Brad M. [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
kinetics; living polymerization; methyl acrylate; radical polymerization; SET-LRP; LIVING RADICAL POLYMERIZATION; ELECTRON-TRANSFER; METHYL ACRYLATE; BLOCK-COPOLYMERS; METAL HALIDE; EQUILIBRIUM; COMPLEXES; DMSO; DISPROPORTIONATION; 25-DEGREES-C;
D O I
10.1002/pola.23689
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
SET-LRP requires a combination of ligand and solvent that mediates the disproportionation of Cu(I)X into Cu(O) activator, and Cu(II) deactivator. The solvent also modulates the kinetics of the reaction. More polar solvents, including mixtures of water and organic solvents enhance the rate of polymerization in accord with the Dimroth-Reichardt parameter. Here, it is demonstrated that a similar effect is observed in binary mixtures of organic solvents, wherein the addition of a more polar solvent to a less polar solvent provides a linear increase in the apparent rate constant of propagation, k(p)(app). However, this linear relationship does not hold for the entire range of volume fraction for binary mixtures when ethylene carbonate (EC) or MeOH are one of the two components. Results herein, suggest that the kinetics of SET-LRP in these solvent mixtures is cooperatively and synergistically determined by polarity, degree of disproportionation, and also by another parameter related to the ability of the solvent to stabilize colloidal Cu(O) and determine its particle size. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5591-5605, 2009
引用
收藏
页码:5591 / 5605
页数:15
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