Abstract
ABSTRACTNovel thioxanthone (TX) derivatives are used as versatile photoinitiators upon visible light‐emitting diode (LED; e.g., 405, 425, and 450 nm) exposure. The mechanisms for the photochemical generation of reactive species (i.e., cations and free radicals) produced from photoinitiating systems based on the photoinitiator and an iodonium salt, tris(trimethylsilyl)silane, or an amine, were studied by UV–vis spectroscopy, fluorescence, cyclic voltammetry, steady‐state photolysis, and electron spin resonance spin‐trapping techniques. The reactive species are particularly efficient for cationic, free radical, hybrid, and thiol‐ene photopolymerizations upon LED exposure. The optimized photoinitiating systems exhibit higher efficiency than those of reference systems (i.e., isopropyl TX‐based photoinitiating systems), especially in the visible range. According to their beneficial features, these photoinitiating systems have considerable potential in photocuring applications. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 4037–4045
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