Dithiocarbamate mediated controlled/living free radical polymerization of methyl acrylate under 60Co γ-ray irradiation:: Conjugation effect of N-group

被引:42
作者
Hua, DB [1 ]
Bai, RK [1 ]
Lu, WQ [1 ]
Pan, CY [1 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, Hefei 230026, Peoples R China
关键词
conjugation; dithiocarbamate; living polymerization; molecular weight distribution; radiation;
D O I
10.1002/pola.20394
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 free radical polymerizations of methyl acrylate have been studied under gamma-ray irradiation in the presence of the dithiocarbamates with different N-groups. The results indicate that the conjugation structure of the N-group of dithiocarbamate plays an important role in living free radical polymerization. The polymerizations reveal good living characteristics in the presence of dithiocarbamates (benzyl 1H-imidazole-l-carbodithioate, benzyl 1H-pyrrole-l-carbodithioate, benzyl 1H-indole1-carbodithioate, and benzyl 9H-carbazole-9-carbodithioate) with N-aryl group. In contrast, the polymerization with benzyl N,N,N-diethyldithiocarbamate cannot be controlled, and the obtained polymer has a broad molecular weight distribution or even crosslink occurs. Moreover, polymerization rate is influenced by the conjugation structure of the N-group of dithiocarbamate, and the aromatic polycyclic structure of the N-group leads to slow polymerization. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:5670 / 5677
页数:8
相关论文
共 39 条
[1]  
Bai RK, 2001, MACROMOL RAPID COMM, V22, P315, DOI 10.1002/1521-3927(20010301)22:5<315::AID-MARC315>3.0.CO
[2]  
2-O
[3]  
Bai RK, 2001, MACROMOL CHEM PHYS, V202, P1970, DOI 10.1002/1521-3935(20010601)202:9<1970::AID-MACP1970>3.0.CO
[4]  
2-Q
[5]   Reversible addition-fragmentation chain transfer polymerization initiated with γ-radiation at ambient temperature:: an overview [J].
Barner, L ;
Quinn, JF ;
Barner-Kowollik, C ;
Vana, P ;
Davis, TP .
EUROPEAN POLYMER JOURNAL, 2003, 39 (03) :449-459
[6]   Reversible addition-fragmentation chain-transfer graft polymerization of styrene: Solid phases for organic and peptide synthesis [J].
Barner, L ;
Zwaneveld, N ;
Perera, S ;
Pham, Y ;
Davis, TP .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (23) :4180-4192
[7]   Long-lived intermediates in reversible addition-fragmentation chain-transfer (RAFT) polymerization generated by γ radiation [J].
Barner-Kowollik, C ;
Vana, P ;
Quinn, JF ;
Davis, TP .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (08) :1058-1063
[8]   Modeling the reversible addition-fragmentation chain transfer process in cumyl dithiobenzoate-mediated styrene homopolymerizations: Assessing rate coefficients for the addition-fragmentation equilibrium [J].
Barner-Kowollik, C ;
Quinn, JF ;
Morsley, DR ;
Davis, TP .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2001, 39 (09) :1353-1365
[9]   The reversible addition-fragmentation chain transfer process and the strength and limitations of modeling: Comment on "the magnitude of the fragmentation rate coefficient" [J].
Barner-Kowollik, C ;
Coote, ML ;
Davis, TP ;
Radom, L ;
Vana, P .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (18) :2828-2832
[10]   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