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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| Vydáno v: | RSC advances Ročník 8; číslo 29; s. 16330 - 16335 |
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| Hlavní autoři: | , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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England
Royal Society of Chemistry
01.01.2018
The Royal Society of Chemistry |
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| ISSN: | 2046-2069, 2046-2069 |
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| Abstract | 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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| AbstractList | 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.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. 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. 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. Two eco-respectful, one-step synthetic routes for the preparation of a bio-based epoxy monomer derived from furan precursors are developed. |
| Author | Ambrogi, Veronica Cerruti, Pierfrancesco Mija, Alice Marotta, Angela |
| Author_xml | – sequence: 1 givenname: Angela surname: Marotta fullname: Marotta, Angela organization: Department of Chemical, Materials and Production Engineering (DICMaPI), University of Naples “Federico II”, 80125 Napoli, Italy – sequence: 2 givenname: Veronica surname: Ambrogi fullname: Ambrogi, Veronica organization: Department of Chemical, Materials and Production Engineering (DICMaPI), University of Naples “Federico II”, 80125 Napoli, Italy – sequence: 3 givenname: Pierfrancesco surname: Cerruti fullname: Cerruti, Pierfrancesco organization: Institute for Polymers, Composites and Biomaterials (IPCB), CNR, 80078 Pozzuoli (NA), Italy – sequence: 4 givenname: Alice orcidid: 0000-0001-5208-5956 surname: Mija fullname: Mija, Alice organization: Université Côte d’Azur, Université Nice-Sophia Antipolis, Institut de Chimie de Nice, UMR CNRS 7272, 06108 Nice Cedex 02, France |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35542187$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Chemistry epoxides furans Monomers thermal properties Thermodynamic properties |
| Title | Green approaches in the synthesis of furan-based diepoxy monomers |
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