首页 | 本学科首页   官方微博 | 高级检索  
     检索      

大分子阳离子光引发剂聚苯乙烯-碘鎓六氟锑酸盐的合成及其感光性能的研究
引用本文:夏朝荣,刘仁,黄强,张胜文,江金强,刘晓亚.大分子阳离子光引发剂聚苯乙烯-碘鎓六氟锑酸盐的合成及其感光性能的研究[J].影像科学与光化学,2008,26(6):438-444.
作者姓名:夏朝荣  刘仁  黄强  张胜文  江金强  刘晓亚
作者单位:江南大学, 化学与材料工程学院, 江苏, 无锡, 214122
摘    要:本文用羟基对甲苯磺酰氧基碘苯与聚苯乙烯进行亲电取代反应,得到大分子阳离子碘鎓盐光引发剂聚苯乙烯碘鎓-六氟锑酸盐(PS-I·SbF6).用核磁共振仪、傅立叶红外光谱仪、凝胶渗透色谱仪、差示扫描量热仪、紫外分光光度仪对其进行了表征.与小分子碘鎓盐系光引发剂相比,PS-I·SbF6的紫外最大吸收波长λmax红移,在240-270 nm范围内有较强的吸收;固化成膜后其相对迁移率较小分子光引发剂有显著下降.初步研究了PS-I·SbF6在环氧体系中的光固化性能,结果表明该体系有较好的光固化和后固化特性.

关 键 词:碘鎓盐  阳离子大分子光引发剂  紫外光固化  感光性能  
收稿时间:2008-01-07

Synthesis and Photoinitiation Activity of a Novel Cationic Macrophotoinitiator Polystyrene-iodonium Hexafluoroantimonate
XIA Chao-rong,LIU Ren,HUANG Qiang,ZHANG Sheng-wen,JIANG Jin-qiang,LIU Xiao-ya.Synthesis and Photoinitiation Activity of a Novel Cationic Macrophotoinitiator Polystyrene-iodonium Hexafluoroantimonate[J].Imaging Science and Photochemistry,2008,26(6):438-444.
Authors:XIA Chao-rong  LIU Ren  HUANG Qiang  ZHANG Sheng-wen  JIANG Jin-qiang  LIU Xiao-ya
Institution:School of Chemical & Material Engineering, Jiangnan University, Wuxi, 214122, Jiangsu, P. R. China
Abstract:In this article,a novel Cationic Macropbotoinitiator Polystyrene-iodonium hexafluoroanti- monate (PS-I·SbF_6) was prepared by the reaction of Polystyrene with hydroxy(tosyloxy)iodo] benzene.The later product PS-I·SbF_6 was identified by ~1H-NMR,FTIR,GPC,DSC,and UV spectrum.The red shift phenomenon was observed in the ultraviolet spectrum of PS-I·SbF_6,itsλ_(max) moved from 227 to 260 nm,so it can well match with mercury lamp.Compared with the small molecular iodonium photoinitiators,its relative migration ratio in the cured film was much lower. The photoinitiation activities of the epoxy system in which PS-I·ShF_6 as a cationic photoinitiator were studied.Results showed that the system had good curing and post-curing ability.
Keywords:iodonium salt  cationic macrophotoinitiator  UV curing  photoinitiation activity
本文献已被 万方数据 等数据库收录!
点击此处可从《影像科学与光化学》浏览原始摘要信息
点击此处可从《影像科学与光化学》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号