2019
DOI: 10.1016/j.porgcoat.2019.06.027
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Multicomponent photoinitiating systems containing arylamino oxime ester for visible light photopolymerization

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Cited by 36 publications
(37 citation statements)
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“…21,25 Recently, several research studies have elegantly reported the significant photopolymerization ability of different OXE's under visible light. [26][27][28][29] Different chromophores were introduced for red-shifting their absorption wavelength for better matching with different LED light sources. In the present paper, never reported OXE's derivatives were synthesized and proposed as highperformance PIS's.…”
Section: Introductionmentioning
confidence: 99%
“…21,25 Recently, several research studies have elegantly reported the significant photopolymerization ability of different OXE's under visible light. [26][27][28][29] Different chromophores were introduced for red-shifting their absorption wavelength for better matching with different LED light sources. In the present paper, never reported OXE's derivatives were synthesized and proposed as highperformance PIS's.…”
Section: Introductionmentioning
confidence: 99%
“…The followed photodecarboxylation can suppress recoupling of the generated free radicals and the released CO 2 might reduce oxygen inhibition . Wang et al., reported a series of phenothiazine‐substituted oxime esters as photocleavable PIs sensitive to 405 nm laser diodes . Our recent work has proven that when integrating the oxime‐ester moiety into a visible light sensitive coumarin skeleton, the N−O bond can be cleaved under 450 nm LED light irradiation or even under 980 nm near infrared laser excitation with assistance of upconversion nanoparticles .…”
Section: Introductionmentioning
confidence: 83%
“…[22] Wang et al, reported a series of phenothiazine-substituted oxime esters as photocleavable PIs sensitive to 405 nm laser diodes. [23,24] Our recent work has proven that when integrating the oxime-ester moiety into a visible light sensitive coumarin skeleton, the NÀ O bond can be cleaved under 450 nm LED light irradiation [25,26] or even under 980 nm near infrared laser excitation with assistance of upconversion nanoparticles. [27] It should be noted that these asymmetric oxime-esters can produce only one active initiation species after photolysis because the initiation ability of the generated primary iminyl radicals is limited.…”
Section: Introductionmentioning
confidence: 99%
“…First, α-Cleavage type (Type I photoinitiator) also called onecomponent photoinitiator, involving direct cleavage under light irradiation to produce initiating radicals. [19,20] Second, hydrogen abstraction type (Type II photoinitiator) also called two-component photoinitiator, involving generation of radicals by hydrogen acceptor and electron/proton transfer processes from hydrogen acceptor to hydrogen donor co-initiator. [21] Among various Type II photoinitiators, benzophenone (BP) is the most widely used hydrogen abstracting compound in short wavelength UV.…”
Section: Introductionmentioning
confidence: 99%