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Synthesis and Analysis of Resorcinol-Acetone Copolymer

Synthesis and characterization of resorcinol-acetone copolymer is described. The polymer was prepared by trifluoroacetic acid-catalyzed polymerization of resorcinol with acetone. According to the (1)H-NMR, (13)C-NMR, and MALDI-TOF Mass spectra data, the obtained polymer had three types of repeating...

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Detalles Bibliográficos
Autores principales: Kobayashi, Ataru, Konishi, Gen-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253941/
https://www.ncbi.nlm.nih.gov/pubmed/19145215
http://dx.doi.org/10.3390/molecules14010364
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author Kobayashi, Ataru
Konishi, Gen-ichi
author_facet Kobayashi, Ataru
Konishi, Gen-ichi
author_sort Kobayashi, Ataru
collection PubMed
description Synthesis and characterization of resorcinol-acetone copolymer is described. The polymer was prepared by trifluoroacetic acid-catalyzed polymerization of resorcinol with acetone. According to the (1)H-NMR, (13)C-NMR, and MALDI-TOF Mass spectra data, the obtained polymer had three types of repeating units: isopropylidene bridged-resorcinol, chromane ring, and spiro-shaped double chromane ring, indicating that polymerization proceeded via simultaneous addition-condensation and cyclization of resorcinol with acetone. The obtained polymer can be useful not only for the development of plastic materials such as thermosets, adhesives, and coatings but also for the synthesis of biomaterials such as antimicrobial agents, pesticides, and medicines.
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spelling pubmed-62539412018-11-30 Synthesis and Analysis of Resorcinol-Acetone Copolymer Kobayashi, Ataru Konishi, Gen-ichi Molecules Article Synthesis and characterization of resorcinol-acetone copolymer is described. The polymer was prepared by trifluoroacetic acid-catalyzed polymerization of resorcinol with acetone. According to the (1)H-NMR, (13)C-NMR, and MALDI-TOF Mass spectra data, the obtained polymer had three types of repeating units: isopropylidene bridged-resorcinol, chromane ring, and spiro-shaped double chromane ring, indicating that polymerization proceeded via simultaneous addition-condensation and cyclization of resorcinol with acetone. The obtained polymer can be useful not only for the development of plastic materials such as thermosets, adhesives, and coatings but also for the synthesis of biomaterials such as antimicrobial agents, pesticides, and medicines. Molecular Diversity Preservation International 2009-01-13 /pmc/articles/PMC6253941/ /pubmed/19145215 http://dx.doi.org/10.3390/molecules14010364 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Kobayashi, Ataru
Konishi, Gen-ichi
Synthesis and Analysis of Resorcinol-Acetone Copolymer
title Synthesis and Analysis of Resorcinol-Acetone Copolymer
title_full Synthesis and Analysis of Resorcinol-Acetone Copolymer
title_fullStr Synthesis and Analysis of Resorcinol-Acetone Copolymer
title_full_unstemmed Synthesis and Analysis of Resorcinol-Acetone Copolymer
title_short Synthesis and Analysis of Resorcinol-Acetone Copolymer
title_sort synthesis and analysis of resorcinol-acetone copolymer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253941/
https://www.ncbi.nlm.nih.gov/pubmed/19145215
http://dx.doi.org/10.3390/molecules14010364
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