Disubstituted Aminoanthraquinone-Based Multicolor Photoinitiators: Photoinitiation Mechanism and Ability of Cationic Polymerization under Blue, Green, Yellow, and Red LEDs
Author(s) -
Jing Zhang,
Jacques Lalevée,
Nicholas S. Hill,
Kévin Launay,
F. Morlet-Savary,
Bernadette Graff,
Martina H. Stenzel,
Michelle L. Coote,
Pu Xiao
Publication year - 2018
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.8b01763
Subject(s) - photopolymer , photochemistry , cationic polymerization , flash photolysis , chemistry , fluorescence , polymerization , photosensitizer , fluorescence spectroscopy , light emitting diode , photoinitiator , photodissociation , quantum yield , monomer , polymer chemistry , materials science , polymer , organic chemistry , kinetics , optoelectronics , optics , physics , quantum mechanics , reaction rate constant
The investigation and clarification of the photoinitiation mechanism of novel systems are of importance for the design and development of compounds with high photoinitiation efficiency of photopolymerization. Some disubstituted aminoanthraquinone derivatives have been reported to exhibit interesting photochemical/photophysical properties and have the potential to act as high performance multicolor photoinitiators under the irradiation of various wavelengths of visible light from light-emitting diodes (LEDs). Herein, three disubstituted aminoanthraquinone derivatives, i.e., 1-amino-4-hydroxyanthraquinone, 1,4-diaminoanthraquinone, and 1,5-diaminoanthraquinone, with iodonium salt and N-vinylcarbazole as additives, have been investigated. Their photoinitiation mechanism was studied using fluorescence spectroscopy, laser flash photolysis, steady state photolysis, computational quantum chemistry, and electron spin resonance spin trapping techniques. Then, their photoinitiation ability for the cationic photopol...
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