Copper(0)-mediated radical polymerization of styrene at room temperature

被引:8
作者
Zhang, Xiao-fei [1 ]
Wu, Yang [1 ]
Huang, Jun [1 ]
Miao, Xue-lang [1 ]
Zhang, Zheng-biao [1 ]
Zhu, Xiu-lin [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Gel permeation chromatography (GPC); Kinetics (polym.); Cu(0)-mediated radical polymerization; Styrene; FLIGHT MASS-SPECTROMETRY; FRAGMENTATION CHAIN TRANSFER; METHYL ACRYLATE; POLYDISPERSE POLYMERS; DMSO; DISCRIMINATION; METHACRYLATE; SET;
D O I
10.1007/s10118-013-1243-6
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 "living'/controlled radical polymerization (LRP) of styrene (St) at room temperature is rarely reported. In this work, copper(0) (Cu(0))-mediated radical polymerization of St at room temperature was investigated in detail. Dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF) as well as a binary solvent, tetrahydrofuran/1,1,1,3,3,3-hexafluoro-2-propanol were used as the solvents, respectively. Methyl-2-bromopropionate and ethyl 2-bromoisobutyrate were used as the initiators, respectively. The polymerization proceeded smoothly with moderate conversions at room temperature. It was found that DMF was a good solvent with the essential features of LRP, while DMSO was a poor solvent with uncontrollable molecular weights. Besides, the match among the initiator, solvent and molar ratios of reactants can modulate the livingness of the polymerization, and the proper selection of ligand was also crucial to a controlled process. This work provided a first example of Cu(0)-mediated radical polymerization of St at room temperature, which would enrich and strength the LRP technique.
引用
收藏
页码:702 / 712
页数:11
相关论文
共 35 条
[1]   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
[2]  
DEADY M, 1993, MAKROMOL CHEM, V194, P1691
[3]   Transition metal catalysts for controlled radical polymerization [J].
di Lena, Fabio ;
Matyjaszewski, Krzysztof .
PROGRESS IN POLYMER SCIENCE, 2010, 35 (08) :959-1021
[4]   Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry interlaboratory comparison of mixtures of polystyrene with different end groups: Statistical analysis of mass fractions and mass moments [J].
Guttman, CM ;
Wetzel, SJ ;
Flynn, KM ;
Fanconi, BM ;
VanderHart, DL ;
Wallace, WE .
ANALYTICAL CHEMISTRY, 2005, 77 (14) :4539-4548
[5]   New polymer synthesis by nitroxide mediated living radical polymerizations [J].
Hawker, CJ ;
Bosman, AW ;
Harth, E .
CHEMICAL REVIEWS, 2001, 101 (12) :3661-3688
[6]   Metal-catalyzed living radical polymerization [J].
Kamigaito, M ;
Ando, T ;
Sawamoto, M .
CHEMICAL REVIEWS, 2001, 101 (12) :3689-3745
[7]   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
[8]   Re(V)-mediated living radical polymerization of styrene:: ReO2I(PPh3)2/R-I initiating systems [J].
Kotani, Y ;
Kamigaito, M ;
Sawamoto, M .
MACROMOLECULES, 1999, 32 (08) :2420-2424
[9]   No Reduction of CuBr2 during Cu(0)-Catalyzed Living Radical Polymerization of Methyl Acrylate in DMSO at 25 °C [J].
Levere, Martin E. ;
Nguyen, Nga H. ;
Percec, Virgil .
MACROMOLECULES, 2012, 45 (20) :8267-8274
[10]   Assessment of SET-LRP in DMSO using online monitoring and Rapid GPC [J].
Levere, Martin E. ;
Willoughby, Ian ;
O'Donohue, Stephen ;
de Cuendias, Anne ;
Grice, Anthony J. ;
Fidge, Christopher ;
Becer, C. Remzi ;
Haddleton, David M. .
POLYMER CHEMISTRY, 2010, 1 (07) :1086-1094