Substituent Effects on Photoinitiation Ability of Coumarin-Based Oxime-Ester Photoinitiators for Free Radical Photopolymerization

Author(s):  
Jacques Lalevée ◽  
Fatima Hammoud ◽  
Nicolas giacoletto ◽  
Guillaume Noirbent ◽  
Bernadette Graff ◽  
...  

In this paper, a series of coumarin chromophore-based oxime-esters was designed and synthesized as visible light photoinitiators (PIs). Interestingly, upon exposure to irradiation of a LED at 405 nm, the...

2001 ◽  
Vol 710 ◽  
Author(s):  
Haruhisa Akiyama ◽  
Nobuyuki Tamaoki

ABSTRACTWe synthesized copolymers of N-isopropylacrylamide (NIPAM) and azobenzene-containing acrylates or acrylamides by free radical polymerization, and investigated the water solubility of these polymers upon irradiation with ultra-violet and visible light. The solubility depended on concentration and structure of photoreactive azobenzene unit in the polymers. The soluble polymers showed the lower critical solution temperature, which was varied along with light irradiation. Photo-induced large wettability alteration was observed in the film.


2020 ◽  
Vol 41 (18) ◽  
pp. 2000166 ◽  
Author(s):  
Jing Zhang ◽  
Jacques Lalevée ◽  
Nicholas S. Hill ◽  
Jonathan Kiehl ◽  
Di Zhu ◽  
...  

2021 ◽  
Vol 12 (9) ◽  
pp. 1286-1297
Author(s):  
Zhong-Han Lee ◽  
Fatima Hammoud ◽  
Akram Hijazi ◽  
Bernadette Graff ◽  
Jacques Lalevée ◽  
...  

Four visible light triphenylamine-based oxime ester photoinitiators (TP-1–4) were synthesized successfully. Photochemical reaction, photoreactivity and 3D pattern experiments were also conducted.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1801
Author(s):  
Tung-Liang Huang ◽  
Yung-Chung Chen

Three novel visible-light absorbing benzophenone-based hydrogen acceptors (BPD-D, BPDM-D and BPDP-D) were designed on the basis of a donor–benzophenone–donor structural backbone. Mono or diketone units and double diphenylamine electron-donating groups in para-or meta-positions were introduced to comprehend the electronic and structural effects on free radical photopolymerization (FRPP). Such a structural change leads not only to a red-shift of the absorption maxima but strongly enhances their molar extinction coefficients compared to the commercial phototinitiators such as benzophenone (BP) and 4,4′-bis(diethylamino) benzophenone (EMK). In addition, excellent melting points and thermal decomposition temperatures were achieved for those novel compounds. Further, the photochemical reaction behavior was studied by cyclic voltammograms (CV), photolysis and electron spin resonance (ESR) spectroscopy. Finally, benzophenone derivatives in combination with an amine (TEA, triethylamine) as a co-initiator were prepared and initiated the FRPP of trimethylolpropane trimethacrylate (TMPTMA) using a UV lamp as a light source. When used in stoichiometric amounts, the BPDP-D/TEA had the best double bond conversion efficiency among all the compounds studied, and were even superior to the reference compounds of BP/TEA and EMK/TEA. The results and conclusions could provide the fundamental rules applicable for the structural design of benzophenone derivative-based photoinitiators.


2021 ◽  
Author(s):  
Davy-Louis Versace ◽  
Louise Breloy ◽  
Yusuf Yagci ◽  
Ismail Yilmaz ◽  
Ozgur Yavuz

Phthalocyanines (Pcs) are interesting molecules offering a fascinating chemistry world which received tremendous interest in the last decade. Their certain features such as high thermal, chemical, and optical stability as...


2021 ◽  
Author(s):  
Jacques Lalevée ◽  
Fatima Hammoud ◽  
Mahmoud Rahal ◽  
Julien Egly ◽  
Fabrice Morlet-Savary ◽  
...  

The investigation of copper-iodide cubane derivatives as new co-initiators for the free radical polymerization (FRP) of acrylate monomers under mild irradiation conditions is described for the first time here. These...


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