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Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer

In this work, we proved the efficient synthesis of a bio-based hyper-branched polyphenol from a modified lignin degradation fragment. Protocatechuic acid was readily obtained from vanillin, a lignin degradation product, via alkaline conditions, and further polymerised to yield high molecular weight...

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Detalles Bibliográficos
Autores principales: Longe, Lionel, Garnier, Gil, Saito, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832395/
https://www.ncbi.nlm.nih.gov/pubmed/31623084
http://dx.doi.org/10.3390/molecules24203717
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author Longe, Lionel
Garnier, Gil
Saito, Kei
author_facet Longe, Lionel
Garnier, Gil
Saito, Kei
author_sort Longe, Lionel
collection PubMed
description In this work, we proved the efficient synthesis of a bio-based hyper-branched polyphenol from a modified lignin degradation fragment. Protocatechuic acid was readily obtained from vanillin, a lignin degradation product, via alkaline conditions, and further polymerised to yield high molecular weight hyperbranched phenol terminated polyesters. Vanillic acid was also subjected to similar polymerisation conditions in order to compare polymerisation kinetics and differences between linear and hyperbranched polymers. Overall, protocatechuic acid was faster to polymerise and more thermostable with a degradation temperature well above linear vanillic acid polyester. Both polymers exhibited important radical scavenging activity (RSA) compared to commercial antioxidant and present tremendous potential for antioxidant applications.
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spelling pubmed-68323952019-11-21 Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer Longe, Lionel Garnier, Gil Saito, Kei Molecules Article In this work, we proved the efficient synthesis of a bio-based hyper-branched polyphenol from a modified lignin degradation fragment. Protocatechuic acid was readily obtained from vanillin, a lignin degradation product, via alkaline conditions, and further polymerised to yield high molecular weight hyperbranched phenol terminated polyesters. Vanillic acid was also subjected to similar polymerisation conditions in order to compare polymerisation kinetics and differences between linear and hyperbranched polymers. Overall, protocatechuic acid was faster to polymerise and more thermostable with a degradation temperature well above linear vanillic acid polyester. Both polymers exhibited important radical scavenging activity (RSA) compared to commercial antioxidant and present tremendous potential for antioxidant applications. MDPI 2019-10-16 /pmc/articles/PMC6832395/ /pubmed/31623084 http://dx.doi.org/10.3390/molecules24203717 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Longe, Lionel
Garnier, Gil
Saito, Kei
Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title_full Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title_fullStr Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title_full_unstemmed Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title_short Synthesis of Lignin-based Phenol Terminated Hyperbranched Polymer
title_sort synthesis of lignin-based phenol terminated hyperbranched polymer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832395/
https://www.ncbi.nlm.nih.gov/pubmed/31623084
http://dx.doi.org/10.3390/molecules24203717
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AT garniergil synthesisofligninbasedphenolterminatedhyperbranchedpolymer
AT saitokei synthesisofligninbasedphenolterminatedhyperbranchedpolymer