Green approaches in the synthesis of furan-based diepoxy monomers

Two eco-respectful, one-step synthetic routes for the preparation of a bio-based epoxy monomer derived from furan precursors are developed. The diglycidyl ester products are throughly characterized in terms of structure and thermal properties. Gathered results indicate that the two selected approach...

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Detalles Bibliográficos
Autores principales: Marotta, Angela, Ambrogi, Veronica, Cerruti, Pierfrancesco, Mija, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080280/
https://www.ncbi.nlm.nih.gov/pubmed/35542187
http://dx.doi.org/10.1039/c8ra02739k
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author Marotta, Angela
Ambrogi, Veronica
Cerruti, Pierfrancesco
Mija, Alice
author_facet Marotta, Angela
Ambrogi, Veronica
Cerruti, Pierfrancesco
Mija, Alice
author_sort Marotta, Angela
collection PubMed
description Two eco-respectful, one-step synthetic routes for the preparation of a bio-based epoxy monomer derived from furan precursors are developed. The diglycidyl ester products are throughly characterized in terms of structure and thermal properties. Gathered results indicate that the two selected approaches allow the preparation of pure, furanic diglycidyl ester, which represents a viable bio-based alternative to its petrochemical aromatic counterpart.
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spelling pubmed-90802802022-05-09 Green approaches in the synthesis of furan-based diepoxy monomers Marotta, Angela Ambrogi, Veronica Cerruti, Pierfrancesco Mija, Alice RSC Adv Chemistry Two eco-respectful, one-step synthetic routes for the preparation of a bio-based epoxy monomer derived from furan precursors are developed. The diglycidyl ester products are throughly characterized in terms of structure and thermal properties. Gathered results indicate that the two selected approaches allow the preparation of pure, furanic diglycidyl ester, which represents a viable bio-based alternative to its petrochemical aromatic counterpart. The Royal Society of Chemistry 2018-05-02 /pmc/articles/PMC9080280/ /pubmed/35542187 http://dx.doi.org/10.1039/c8ra02739k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Marotta, Angela
Ambrogi, Veronica
Cerruti, Pierfrancesco
Mija, Alice
Green approaches in the synthesis of furan-based diepoxy monomers
title Green approaches in the synthesis of furan-based diepoxy monomers
title_full Green approaches in the synthesis of furan-based diepoxy monomers
title_fullStr Green approaches in the synthesis of furan-based diepoxy monomers
title_full_unstemmed Green approaches in the synthesis of furan-based diepoxy monomers
title_short Green approaches in the synthesis of furan-based diepoxy monomers
title_sort green approaches in the synthesis of furan-based diepoxy monomers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080280/
https://www.ncbi.nlm.nih.gov/pubmed/35542187
http://dx.doi.org/10.1039/c8ra02739k
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AT cerrutipierfrancesco greenapproachesinthesynthesisoffuranbaseddiepoxymonomers
AT mijaalice greenapproachesinthesynthesisoffuranbaseddiepoxymonomers

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