Trifunctional Photoinitiators Based on a Triazine Skeleton for Visible Light Source and UV LED Induced Polymerizations

被引:73
作者
Tehfe, Mohamad-Ali [1 ]
Dumur, Frederic [2 ]
Graff, Bernadette [1 ]
Morlet-Savary, Fabrice [1 ]
Fouassier, Jean-Pierre [3 ]
Gigmes, Didier [2 ]
Lalevee, Jacques [1 ]
机构
[1] ENSCMu UHA, LRC CNRS 7228, Inst Sci Mat Mulhouse IS2M, F-68057 Mulhouse, France
[2] Aix Marseille Univ, CNRS, Inst Chim Radicalaire, UMR 7273, F-13397 Marseille, France
[3] UHA ENSCMu, F-68093 Mulhouse, France
关键词
INDUCED CATIONIC-POLYMERIZATION; FREE-RADICAL POLYMERIZATION; THIOXANTHONE-ANTHRACENE; CENTERED RADICALS; AERATED MEDIA; REACTIVITY; PHOTOPOLYMERIZATION; COINITIATORS; EFFICIENCY; RING;
D O I
10.1021/ma301931p
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Trifunctional photoinitiators (tPIs) based on benzophenone, anthracene, and pyrene chromophores linked to a triazine moiety are proposed as new initiating systems. In combination with an iodonium salt and a silane, these structures are able to initiate the radical polymerization RP of acrylates and the cationic polymerization CP of epoxides and vinylethers under Xe-Hg lamp, LED and very soft irradiation (i.e., halogen lamp). Upon addition of an amine, these new photoinitiators were also able to start the radical polymerization of acrylates. Excellent RP and CP polymerization profiles are obtained i.e. better than those recorded using the reference compounds (benzophenone, anthracence and pyrene). In CP, some of these compounds combined with thianthrenium salts can also be used The mechanisms involved in the different multicomponent initiating systems were analyzed by ESR, fluorescence, steady state photolysis, and laser flash photolysis experiments.
引用
收藏
页码:8639 / 8647
页数:9
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