Kim Young-Jin, Uyama Hiroshi, Kobayashi Shiro
Department of Materials Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan.
Macromol Biosci. 2004 May 17;4(5):497-502. doi: 10.1002/mabi.200300078.
Peroxidase-catalyzed oxidative polymerization of phenol has been examined using the template, poly(ethylene glycol) monododecyl ether (PEGMDE), in water. The role of this template, which forms a complex with phenol in the polymerization, was verified by UV measurements. During the reaction, a complex of the resulting polymer and PEGMDE was precipitated in high yields. The amount and the PEG chain length of PEGMDE strongly affected the polyphenol yield. The unit molar ratio of polyphenol and PEG of the template was about 1:0.9. The presence of the PEGMDE template in the aqueous medium greatly improved the regioselectivity of the polymerization, yielding polyphenol with a phenylene unit content close to 90%. FT-IR, DSC, and XRD analyses confirmed the formation of the miscible complex of polyphenol and PEGMDE by hydrogen-bonding interactions.
已在水中使用模板聚乙二醇单十二烷基醚(PEGMDE)研究了过氧化物酶催化的苯酚氧化聚合反应。通过紫外测量验证了该模板在聚合反应中与苯酚形成络合物的作用。反应过程中,所得聚合物与PEGMDE的络合物以高产率沉淀。PEGMDE的用量和聚乙二醇链长对多酚产率有很大影响。模板中多酚与聚乙二醇的单位摩尔比约为1:0.9。水性介质中PEGMDE模板的存在极大地提高了聚合反应的区域选择性,得到亚苯基单元含量接近90%的多酚。傅里叶变换红外光谱(FT-IR)、差示扫描量热法(DSC)和X射线衍射(XRD)分析证实了多酚与PEGMDE通过氢键相互作用形成了可混溶络合物。