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Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines
With the aim of obtaining halogen-free polybenzoxazazines with reduced flammability, phosphazene-containing benzoxazines (PhBZ) were synthesized in a two-stage method. In the first stage of the reaction of hexachlorocycotriphosphazene with bisphenol A at molar ratios of 1:12, 1:16, and 1:24, respect...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361955/ https://www.ncbi.nlm.nih.gov/pubmed/32481501 http://dx.doi.org/10.3390/polym12061225 |
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author | Sirotin, Igor S. Sarychev, Igor A. Vorobyeva, Viktoria V. Kuzmich, Anastasia A. Bornosuz, Natalia V. Onuchin, Denis V. Gorbunova, Irina Yu. Kireev, Vyacheslav V. |
author_facet | Sirotin, Igor S. Sarychev, Igor A. Vorobyeva, Viktoria V. Kuzmich, Anastasia A. Bornosuz, Natalia V. Onuchin, Denis V. Gorbunova, Irina Yu. Kireev, Vyacheslav V. |
author_sort | Sirotin, Igor S. |
collection | PubMed |
description | With the aim of obtaining halogen-free polybenzoxazazines with reduced flammability, phosphazene-containing benzoxazines (PhBZ) were synthesized in a two-stage method. In the first stage of the reaction of hexachlorocycotriphosphazene with bisphenol A at molar ratios of 1:12, 1:16, and 1:24, respectively, mixtures of bisphenol and hydroxyaryloxycyclotriphosphazenes were obtained, which mainly contained P(3)N(3)[OC(6)H(4)C(CH(3))(3)C(6)H(4)OH](6). In the second stage, when these mixtures interacted with aniline and an excess of paraformaldehyde in toluene at 80–90 °C, PhBZ containing 20–50% of the phosphazene component with M(w) 1200–5800 were formed. According to (1)H and (13)C NMR spectroscopy, PhBZ contain a small amount of oligomeric compounds with Mannich aminomethylene bridges. With an increase of the content of the phosphazene component, the curing temperature of PhBZ decreases from 242 °C to 215 °C. Cured PhBZ samples with a phosphorus content of more than 1.5% have increased flammability resistance according to UL-94. |
format | Online Article Text |
id | pubmed-7361955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73619552020-07-21 Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines Sirotin, Igor S. Sarychev, Igor A. Vorobyeva, Viktoria V. Kuzmich, Anastasia A. Bornosuz, Natalia V. Onuchin, Denis V. Gorbunova, Irina Yu. Kireev, Vyacheslav V. Polymers (Basel) Article With the aim of obtaining halogen-free polybenzoxazazines with reduced flammability, phosphazene-containing benzoxazines (PhBZ) were synthesized in a two-stage method. In the first stage of the reaction of hexachlorocycotriphosphazene with bisphenol A at molar ratios of 1:12, 1:16, and 1:24, respectively, mixtures of bisphenol and hydroxyaryloxycyclotriphosphazenes were obtained, which mainly contained P(3)N(3)[OC(6)H(4)C(CH(3))(3)C(6)H(4)OH](6). In the second stage, when these mixtures interacted with aniline and an excess of paraformaldehyde in toluene at 80–90 °C, PhBZ containing 20–50% of the phosphazene component with M(w) 1200–5800 were formed. According to (1)H and (13)C NMR spectroscopy, PhBZ contain a small amount of oligomeric compounds with Mannich aminomethylene bridges. With an increase of the content of the phosphazene component, the curing temperature of PhBZ decreases from 242 °C to 215 °C. Cured PhBZ samples with a phosphorus content of more than 1.5% have increased flammability resistance according to UL-94. MDPI 2020-05-28 /pmc/articles/PMC7361955/ /pubmed/32481501 http://dx.doi.org/10.3390/polym12061225 Text en © 2020 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 Sirotin, Igor S. Sarychev, Igor A. Vorobyeva, Viktoria V. Kuzmich, Anastasia A. Bornosuz, Natalia V. Onuchin, Denis V. Gorbunova, Irina Yu. Kireev, Vyacheslav V. Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title_full | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title_fullStr | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title_full_unstemmed | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title_short | Synthesis of Phosphazene-Containing, Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines |
title_sort | synthesis of phosphazene-containing, bisphenol a-based benzoxazines and properties of corresponding polybenzoxazines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361955/ https://www.ncbi.nlm.nih.gov/pubmed/32481501 http://dx.doi.org/10.3390/polym12061225 |
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