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Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures

3,4-dihydro-3-phenyl-2H-1,3-benzoxazines derived from phenol-, resorcinol-, and phloroglucinol give monomers with one, two, and three oxazine units at a single benzene ring, respectively. Aside from the synthesis and characterization of such multifunctional benzoxazines, reactivity and polymerizatio...

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Detalles Bibliográficos
Autores principales: Soto, Marc, Hiller, Matthias, Oschkinat, Hartmut, Koschek, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432505/
https://www.ncbi.nlm.nih.gov/pubmed/30974555
http://dx.doi.org/10.3390/polym8080278
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author Soto, Marc
Hiller, Matthias
Oschkinat, Hartmut
Koschek, Katharina
author_facet Soto, Marc
Hiller, Matthias
Oschkinat, Hartmut
Koschek, Katharina
author_sort Soto, Marc
collection PubMed
description 3,4-dihydro-3-phenyl-2H-1,3-benzoxazines derived from phenol-, resorcinol-, and phloroglucinol give monomers with one, two, and three oxazine units at a single benzene ring, respectively. Aside from the synthesis and characterization of such multifunctional benzoxazines, reactivity and polymerization behavior is studied in dependence of the oxazine functionality. Monomer reactivities are directly related to the number of oxazine functionalities present at the benzene ring yielding the lowest polymerization temperature for the trifunctional phloroglucinol-based benzoxazine. Comparing the polymerization processes and resulting structures, the trifunctional benzoxazine derivative enter new polymerization pathways, which include methylene linkages bridging aniline units, as well as the formation of carbonyl-derived structures.
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spelling pubmed-64325052019-04-02 Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures Soto, Marc Hiller, Matthias Oschkinat, Hartmut Koschek, Katharina Polymers (Basel) Article 3,4-dihydro-3-phenyl-2H-1,3-benzoxazines derived from phenol-, resorcinol-, and phloroglucinol give monomers with one, two, and three oxazine units at a single benzene ring, respectively. Aside from the synthesis and characterization of such multifunctional benzoxazines, reactivity and polymerization behavior is studied in dependence of the oxazine functionality. Monomer reactivities are directly related to the number of oxazine functionalities present at the benzene ring yielding the lowest polymerization temperature for the trifunctional phloroglucinol-based benzoxazine. Comparing the polymerization processes and resulting structures, the trifunctional benzoxazine derivative enter new polymerization pathways, which include methylene linkages bridging aniline units, as well as the formation of carbonyl-derived structures. MDPI 2016-08-02 /pmc/articles/PMC6432505/ /pubmed/30974555 http://dx.doi.org/10.3390/polym8080278 Text en © 2016 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
Soto, Marc
Hiller, Matthias
Oschkinat, Hartmut
Koschek, Katharina
Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title_full Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title_fullStr Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title_full_unstemmed Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title_short Multifunctional Benzoxazines Feature Low Polymerization Temperature and Diverse Polymer Structures
title_sort multifunctional benzoxazines feature low polymerization temperature and diverse polymer structures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432505/
https://www.ncbi.nlm.nih.gov/pubmed/30974555
http://dx.doi.org/10.3390/polym8080278
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