Un fotoiniciador bifuncional de benzofenona-carbazol tipo II monocomponente para sistemas fotoiniciadores LED

Autor: Fabrice Morlet-Savary, Damien Brunel, Shaohui Liu, Yangyang Xu, Ke Sun, Jacques Lalevée, Pu Xiao, Bernadette Graff, Frédéric Dumur
Přispěvatelé: Institut de Science des Matériaux de Mulhouse (IS2M), Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie Radicalaire (ICR), Aix Marseille Université (AMU)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Research School of Chemistry, Australian National University (ANU), Centre National de la Recherche Scientifique (CNRS)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique, Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Polymer Chemistry
Polymer Chemistry, 2020, 11 (21), pp.3551-3556. ⟨10.1039/D0PY00644K⟩
Polymer Chemistry, Royal Society of Chemistry-RSC, 2020, 11 (21), pp.3551-3556. ⟨10.1039/D0PY00644K⟩
ISSN: 1759-9954
1759-9962
DOI: 10.1039/D0PY00644K⟩
Popis: International audience; A bifunctional benzophenone-carbazole-based photoinitiator BPC was designed from its molecular structure viewpoint. To get this, two benzoyl substituents were introduced as peripheral groups of carbazole so that a molecule in which two benzophenones were fused to one carbazole unit could be obtained in a one-step procedure. As a result of this combination, synergetic effects are thus attended. Interestingly, BPC could efficiently initiate the free radical photopolymerization (FRP) of acrylates without addition of any extra hydrogen donors demonstrating a monocomponent Type II behavior but also fast photoinitiation rates were obtained in the presence of an amine and/or an iodonium salt with a LED@365 nm. Meanwhile, BPC can also interact with the iodonium salt to generate cationic species for the cationic photopolymerization (CP) of epoxides. BPC was found as a versatile photoinitiator that can be used for both radical and cationic polymerizations. The best photoinitiating system (PIS) determined during the FRP tests was selected for 3D printing experiments. Steady state photolysis and fluorescence quenching experiments were carried out to verify the interaction between BPC and the different additives in the excited state. Electron spin resonance-spin trapping experiments successfully distinguished the free radicals generated by the different PISs and the proposed electron transfer mechanisms
Databáze: OpenAIRE