GARBAY, Guillaume; GIRAUD, Lauriane; GALI, Sai Manoj; HADZIIOANNOU, Georges; GRAU, Etienne; GRELIER, Stéphane; CLOUTET, Eric; CRAMAIL, Henri; BROCHON, Cyril

doi:10.1021/acsomega.9b04181

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GARBAY, Guillaume
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies

GIRAUD, Lauriane
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies

GALI, Sai Manoj
Institut des Sciences Moléculaires [ISM]
Laboratoire de Chimie des Polymères Organiques [LCPO]
Team 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies

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ACS Omega. 2020

ACS Publications

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2020

Résumé en anglais

Divanillin was synthesized in high yield and purity using Laccase from Trametes versicolor. It was then pol-ymerized with Benzene-1,4-diamine and 2,7-diaminocarbazole to form polyazomethines. Polymerizations were performed under microwave irradiation and without transition-metal based catalyst. These bio-based conjugated polyazomethines present a broad fluorescence spectrum ranging from 400 to 600 nm. Depending on the co-monomer used, polyazomethines with molar masses around 10 kg.mol-1 and with electronic gaps ranging from 2.66 to 2.85 eV were obtained. Furthermore, TD-DFT calculations were performed to corroborate experimental results.< Réduire

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Polyazomethines

Carbazole

Divanillin

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Divanillin-Based Polyazomethines: Toward Biobased and Metal-Free π-Conjugated Polymers

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