Cargando…

Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds

The synthesis of π-conjugated polymers via an environmentally friendly procedure is generally challenging. Herein, we describe the synthesis of divanillin-based polyazomethines, which are derived from a potentially bio-based monomer. The polymerization is performed in 5 min under microwave irradiati...

Descripción completa

Detalles Bibliográficos
Autores principales: Giraud, Lauriane, Grelier, Stéphane, Grau, Etienne, Garel, Laurent, Hadziioannou, Georges, Kauffmann, Brice, Cloutet, Éric, Cramail, Henri, Brochon, Cyril
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268122/
https://www.ncbi.nlm.nih.gov/pubmed/35807392
http://dx.doi.org/10.3390/molecules27134138
_version_ 1784743899180302336
author Giraud, Lauriane
Grelier, Stéphane
Grau, Etienne
Garel, Laurent
Hadziioannou, Georges
Kauffmann, Brice
Cloutet, Éric
Cramail, Henri
Brochon, Cyril
author_facet Giraud, Lauriane
Grelier, Stéphane
Grau, Etienne
Garel, Laurent
Hadziioannou, Georges
Kauffmann, Brice
Cloutet, Éric
Cramail, Henri
Brochon, Cyril
author_sort Giraud, Lauriane
collection PubMed
description The synthesis of π-conjugated polymers via an environmentally friendly procedure is generally challenging. Herein, we describe the synthesis of divanillin-based polyazomethines, which are derived from a potentially bio-based monomer. The polymerization is performed in 5 min under microwave irradiation without any metallic catalyst, with water as the only by-product. The vanillin-based polyazomethines were characterized by SEC, TGA, and UV-Vis spectroscopy. Model compounds were designed and characterized by X-ray diffraction and UV-Vis spectroscopy. The structure/properties study of vanillin-based azomethines used as models allowed us to unequivocally confirm the E configuration and to highlight the cross-conjugated nature of divanillin-based polymers.
format Online
Article
Text
id pubmed-9268122
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92681222022-07-09 Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds Giraud, Lauriane Grelier, Stéphane Grau, Etienne Garel, Laurent Hadziioannou, Georges Kauffmann, Brice Cloutet, Éric Cramail, Henri Brochon, Cyril Molecules Article The synthesis of π-conjugated polymers via an environmentally friendly procedure is generally challenging. Herein, we describe the synthesis of divanillin-based polyazomethines, which are derived from a potentially bio-based monomer. The polymerization is performed in 5 min under microwave irradiation without any metallic catalyst, with water as the only by-product. The vanillin-based polyazomethines were characterized by SEC, TGA, and UV-Vis spectroscopy. Model compounds were designed and characterized by X-ray diffraction and UV-Vis spectroscopy. The structure/properties study of vanillin-based azomethines used as models allowed us to unequivocally confirm the E configuration and to highlight the cross-conjugated nature of divanillin-based polymers. MDPI 2022-06-28 /pmc/articles/PMC9268122/ /pubmed/35807392 http://dx.doi.org/10.3390/molecules27134138 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giraud, Lauriane
Grelier, Stéphane
Grau, Etienne
Garel, Laurent
Hadziioannou, Georges
Kauffmann, Brice
Cloutet, Éric
Cramail, Henri
Brochon, Cyril
Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title_full Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title_fullStr Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title_full_unstemmed Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title_short Synthesis and Characterization of Vanillin-Based π-Conjugated Polyazomethines and Their Oligomer Model Compounds
title_sort synthesis and characterization of vanillin-based π-conjugated polyazomethines and their oligomer model compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268122/
https://www.ncbi.nlm.nih.gov/pubmed/35807392
http://dx.doi.org/10.3390/molecules27134138
work_keys_str_mv AT giraudlauriane synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT grelierstephane synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT grauetienne synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT garellaurent synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT hadziioannougeorges synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT kauffmannbrice synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT clouteteric synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT cramailhenri synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds
AT brochoncyril synthesisandcharacterizationofvanillinbasedpconjugatedpolyazomethinesandtheiroligomermodelcompounds