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新型喹啉衍生物类单体与苯乙烯的原子转移自由基共聚及荧光性能研究
引用本文:文小伟,路建美,徐庆锋,夏雪伟,王丽华.新型喹啉衍生物类单体与苯乙烯的原子转移自由基共聚及荧光性能研究[J].高分子材料科学与工程,2007,23(4):52-55.
作者姓名:文小伟  路建美  徐庆锋  夏雪伟  王丽华
作者单位:苏州大学化学化工学院,江苏,苏州,215123;苏州大学化学化工学院,江苏,苏州,215123;江苏工业学院,江苏,常州,213016
基金项目:国家自然科学基金资助项目(20571054,20476066),江苏省自然科学基金资助项目(BK2005031),江苏省高新技术(BG2005021)
摘    要:合成了一种新型的喹啉衍生物类单体2,7,7-三甲基-3-乙氧羰基-4-(4-丙烯酰胺苯基)-5-氧代-1,4,5,6,7,8-六氢喹啉(TEOHQ),并通过原子转移自由基聚合(ATRP)的方法制备了TEOHQ与苯乙烯的共聚物。以元素分析,GPC,1H-NMR及荧光发射光谱表征了共聚物。数均分子量(M-n)随转化率的线性增加及相对较窄的分子量分布(M-w/M-n)证明了聚合的可控性。同时,利用Mayo-Lewis公式测定了两种单体的竞聚率。最后,从共聚物荧光发射光谱图中显示出共聚物的最大发射峰位于436 nm处,相对于425 nm处单体TEOHQ的最大发射峰发生了11nm的红移。

关 键 词:原子转移自由基聚合  聚喹啉  竞聚率  荧光性能
文章编号:1000-7555(2007)04-052-04
修稿时间:2006-05-19

Atom Transfer Radical Copolymerization of a Novel Quinoline Derivative Monomer with Styrene and Fluorescent Property
WEN Xiao-wei,LU Jian-mei,XU Qing-feng,XIA Xue-wei,WANG Li-hua.Atom Transfer Radical Copolymerization of a Novel Quinoline Derivative Monomer with Styrene and Fluorescent Property[J].Polymer Materials Science & Engineering,2007,23(4):52-55.
Authors:WEN Xiao-wei  LU Jian-mei  XU Qing-feng  XIA Xue-wei  WANG Li-hua
Affiliation:1. Department of Chemistry and Chemical Engineering, Suzhou University, Suzhou 215123, China; 2. Jiangsu Polytechnic University, Changzhou 213016, China
Abstract:A novel quinoline derivative monomer 2,2,7-trimethyl-3-ethoxycarbonyl-4-(4-acrylamidephenyl)-5-oxo-1,4,5,6,7,8hexhydricquinoline(TEOHQ) was synthesized.The copolymers were prepared by atom transfer radical copolymerization of TEOHQ with styrene.Element analysis,GPC,1H-NMR and fluorescent emission spectroscopy were used to characterize copolymers.The linear increase of number average molecular weight(n) versus conversion and the relatively narrow molecular weight distribution(w/n) confirmed that the copolymerization is controllable.In addition,the reactivity ratios of the monomers TEOHQ and styrene were also measured by the method of Mayo-Lewis.Moreover,we investigated the fluorescent property of the obtained copolymers and these copolymers were exhibited fluorescent emission maxima at 436 nm,there is 11nm red-shift comparing to the monomer TEOHQ(425nm).
Keywords:ATRP  polyquinoline  reactivity ratio  fluorescent property
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