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Furan-Indole-Chromenone-Based Organic Photocatalyst for α-Arylation of Enol Acetate and Free Radical Polymerization Under LED Irradiation

Title: Furan-Indole-Chromenone-Based Organic Photocatalyst for α-Arylation of Enol Acetate and Free Radical Polymerization Under LED Irradiation
Authors: Galibert-Guijarro, Aurélien; Noon, Adel; Toufaily, Joumana; Hamieh, Tayssir; Besson, Eric; Gastaldi, Stéphane; Lalevée, Jacques; Feray, Laurence
Source: Galibert-Guijarro, A, Noon, A, Toufaily, J, Hamieh, T, Besson, E, Gastaldi, S, Lalevée, J & Feray, L 2025, 'Furan-Indole-Chromenone-Based Organic Photocatalyst for α-Arylation of Enol Acetate and Free Radical Polymerization Under LED Irradiation', Molecules, vol. 30, no. 2, 265. https://doi.org/10.3390/molecules30020265
Publication Year: 2025
Collection: Maastricht University Research Publications
Subject Terms: alkene arylation; free radical polymerization; organic photocatalyst; photoinduced electron transfer; photoredox catalysis; redox potential
Description: In this study we report on the efficiency of a furane-indole-chromenone-based organic derivative ( ) as a photocatalyst in the a-arylation of enol acetate upon LED irradiation at 405 nm, and as a photoinitiator/photocatalyst in the free radical polymerization of an acrylate group in the presence of -(4- -butylphenyl)iodonium hexafluorophosphate (Iod) as an additive, or in the presence of both Iod and ethyl-4-(dimethyl amino) benzoate (EDB) under LED irradiation at 365 nm. The photochemical properties of this new light-sensitive compound are described, and the wide redox window (3.27 eV) and the high excited-state potentials / (+2.64 V vs. SCE) and / (-2.41 V vs. SCE) offered by this photocatalyst are revealed. The chemical mechanisms that govern the radical chemistry are discussed by means of different techniques, including fluorescence-quenching experiments, UV-visible absorption and fluorescence spectroscopy, and cyclic voltammetry analysis.
Document Type: article in journal/newspaper
Language: English
ISSN: 1420-3049
Relation: info:eu-repo/semantics/altIdentifier/pissn/1420-3049
DOI: 10.3390/molecules30020265
Availability: https://cris.maastrichtuniversity.nl/en/publications/5107953c-336d-4e00-875e-d93f85173e53; https://doi.org/10.3390/molecules30020265
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.42E7560B
Database: BASE