Effect of phenol and derivatives on atom transfer radical polymerization in the presence of air

被引:90
作者
Gnanou, Y
Hizal, G
机构
[1] Univ Bordeaux 1, CNRS, ENSCPB, Lab Chim Polymeres Organ, F-33402 Talence, France
[2] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
关键词
atom transfer radical polymerization; methyl methacrylate; styrene; methyl acrylate; phenol derivatives;
D O I
10.1002/pola.11003
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 various phenolic compounds in conjunction with Cu(II) or Cu(l)N,N,N',N')V'-pentamethyl diethylenetriamine (PMDETA) complexes are used to initiate atom transfer radical polymerization (ATRP) of methyl methacrylate, styrene, and methyl acrylate in the presence of a limited amount of air at temperatures in the range of 80-110 degreesC. Meanwhile, an effort is directed toward the elucidation of the role of phenol and derivatives in ATRP catalyzed by Cu(II)/PMDETA. The catalytic sequence involves the formation of Cu(I) by electron transfer from phenol to Cu(II); Cu(I) so formed can then react in two distinctly different ways: with organic halide to form a propagating radical or with oxygen to form copper salt in its higher oxidation state; and regeneration of Cu(I) by excess phenol. Such regeneration of Cu(I) would be expected to lead to polymerization as a result of the consumption of oxygen and phenol as well. The phenols with electron releasing groups tended to increase the conversion of the polymerization. In this respect, sodium phenoxide, a more effective additive was found, whereas p-nitro phenol was the least effective. The obtained polymers displayed the common features of a controlled polymerization such as molecular weight control and low polydispersity index value (M-w/M-n < 1.5). (C) 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 351-359, 2004
引用
收藏
页码:351 / 359
页数:9
相关论文
共 27 条
[1]   Adventitious effect of air in atom transfer radical polymerization: Air-induced (reverse) atom transfer radical polymerization of methacrylates in the absence of an added initiator [J].
Acar, AE ;
Yagci, MB ;
Mathias, LJ .
MACROMOLECULES, 2000, 33 (21) :7700-7706
[2]   Living radical polymerization of methyl methacrylate with ruthenium complex: Formation of polymers with controlled molecular weights and very narrow distributions [J].
Ando, T ;
Kato, M ;
Kamigaito, M ;
Sawamoto, M .
MACROMOLECULES, 1996, 29 (03) :1070-1072
[3]  
[Anonymous], J CHEM COMMUN
[4]   OXIDATIVE COUPLING POLYMERIZATION OF 2,6-DIMETHYLPHENOL CATALYZED BY COPPER(II) COMPLEXES OF N-METHYLIMIDAZOLE [J].
CHEN, W ;
CHALLA, G .
EUROPEAN POLYMER JOURNAL, 1990, 26 (11) :1211-1216
[5]   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
[6]   Kinetic investigation of the atom transfer radical polymerization of methyl acrylate [J].
Davis, KA ;
Paik, HJ ;
Matyjaszewski, K .
MACROMOLECULES, 1999, 32 (06) :1767-1776
[7]   POLYMERIZATION BY OXIDATIVE COUPLING .5. CATALYTIC SPECIFICITY IN COPPER-AMINE-CATALYZED OXIDATION OF 2,6-DIMETHYLPHENOL [J].
ENDRES, GF ;
EUSTANCE, JW ;
HAY, AS .
JOURNAL OF ORGANIC CHEMISTRY, 1963, 28 (05) :1300-&
[8]   NARROW MOLECULAR-WEIGHT RESINS BY A FREE-RADICAL POLYMERIZATION PROCESS [J].
GEORGES, MK ;
VEREGIN, RPN ;
KAZMAIER, PM ;
HAMER, GK .
MACROMOLECULES, 1993, 26 (11) :2987-2988
[9]   Controlled radical polymerization of methacrylic monomers in the presence of a bis(ortho-chelated) arylnickel(II) complex and different activated alkyl halides [J].
Granel, C ;
Dubois, P ;
Jerome, R ;
Teyssie, P .
MACROMOLECULES, 1996, 29 (27) :8576-8582
[10]   Copper diimine complexes:: the synthesis and crystal structures of [Cu(C10H14N2)2(MeOH)][BF4], [Cu(C10H20N2)2]Br, [{(C10H14N2)CuBr(μ-OMe)}2(MeOH)] and [{(C10H20N2)CuBr(μ-OMe)}2] [J].
Haddleton, DM ;
Clark, AJ ;
Duncalf, DJ ;
Heming, AM ;
Kukulj, D ;
Shooter, AJ .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (03) :381-385