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Highly conjugated visible and near-infrared light photoinitiating systems for radical and cationic polymerizations
[Display omitted] •Novel highly conjugated thiophene derivatives as visible and NIR light sensitizers.•Photoinduced electron transfer reactions between iodonium salt and sensitizers.•Use of incandescent infrared light, photosensitizers and diphenyl iodonium salt for photopolymerization of various mo...
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Published in: | Progress in organic coatings 2021-05, Vol.154, p.106189, Article 106189 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Novel highly conjugated thiophene derivatives as visible and NIR light sensitizers.•Photoinduced electron transfer reactions between iodonium salt and sensitizers.•Use of incandescent infrared light, photosensitizers and diphenyl iodonium salt for photopolymerization of various monomers.•Ability to form hybrid cross-linked polymers.
In this communication, we report highly conjugated thiophenes having [1,2,5]-thiadiazolo and [1,2,5]-selenadiazolo [3,4-f]-benzo [1,2,3] triazole in conjunction with diphenyliodonium hexafluorophosphate salt (DPI) as new visible and near-infrared light (NIR) photoinitiator systems for free radical (FRP) and cationic polymerizations (CP). The postulated mechanism is based on the electron transfer reactions between the excited conjugated molecule and DPI ions. The radicals and Bronsted acid formed this way initiate FRP and CP of appropriate monomers such as methylacrylate (MA), methyl methacrylate (MMA), triethylene glycol dimethacrylate (TEGDMA) and cyclohexene oxide (CHO), isobutyl vinylether (IBVE) respectively. The possibility of in situ hybrid polymerization is also demonstrated using bifunctional monomer glycidyl methacrylate (GMA). |
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ISSN: | 0300-9440 1873-331X |
DOI: | 10.1016/j.porgcoat.2021.106189 |