Radical-controlled oxidative polymerization of 4-phenoxyphenol catalyzed by a dicopper complex of a dinucleating ligand

被引:17
作者
Higashimura, H [1 ]
Kubota, M
Shiga, A
Kodera, M
Uyama, H
Kobayashi, S
机构
[1] Japan Chem Innovat Inst, Joint Res Ctr Precis Polymerizat, Tsukuba, Ibaraki 3058565, Japan
[2] Sumitomo Chem Co Ltd, Tsukuba, Ibaraki 3003294, Japan
[3] Doshisha Univ, Fac Engn, Dept Mol Sci & Technol, Kyotanabe 6100394, Japan
[4] Kyoto Univ, Grad Sch Engn, Dept Chem Mat, Kyoto 6068501, Japan
[5] Natl Inst Mat & Chem Res, Tsukuba, Ibaraki 3058565, Japan
关键词
oxidative polymerization; 4-phenoxyphenol; dicopper complex; dinucleating ligand;
D O I
10.1016/S1381-1169(00)00314-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The oxidative polymerization of 4-phenoxyphenol (PPL) catalyzed by a dicopper complex with a dinucleating ligand, 1,2-bis[2-(bis(2-pyridyl)methyl)-6-pyridyl]ethane is described. The polymerization proceeded regioselectively to give crystalline unsubstituted poly(1,4-phenylene oxide) (PPO), in which mu-eta(2):eta(2)-peroxo dicopper(II) species is probably involved as the active dioxygen intermediate. A copper complex with a mononucleating ligand of the similar structure, I,1,l-tris(6-methylpyrid-2-yl)ethane, also catalyzed the oxidative coupling of PPL. The coupling selectivity for the dicopper/dinucleating ligand complex was close to that for the copper/mononucleating ligand complex. However, the initial reaction rate for the former was independent on the catalyst amount in a certain range, whereas that for the latter decreased with the decrease of the catalyst amount. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:233 / 237
页数:5
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