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Solvent-free synthesis and characterization of allyl chitosan derivatives
The solvent-free synthesis of allyl-substituted chitosan derivatives through reactive co-extrusion of chitosan powder with allyl bromide at shear deformation was performed. For the structural characterization, FTIR and NMR methods were employed. The results were confirmed by chemical analysis. The t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066023/ https://www.ncbi.nlm.nih.gov/pubmed/35515576 http://dx.doi.org/10.1039/c9ra03830b |
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author | Akopova, Tatiana A. Demina, Tatiana S. Cherkaev, Georgii V. Khavpachev, Mukhamed A. Bardakova, Kseniya N. Grachev, Andrey V. Vladimirov, Leonid V. Zelenetskii, Alexander N. Timashev, Petr S. |
author_facet | Akopova, Tatiana A. Demina, Tatiana S. Cherkaev, Georgii V. Khavpachev, Mukhamed A. Bardakova, Kseniya N. Grachev, Andrey V. Vladimirov, Leonid V. Zelenetskii, Alexander N. Timashev, Petr S. |
author_sort | Akopova, Tatiana A. |
collection | PubMed |
description | The solvent-free synthesis of allyl-substituted chitosan derivatives through reactive co-extrusion of chitosan powder with allyl bromide at shear deformation was performed. For the structural characterization, FTIR and NMR methods were employed. The results were confirmed by chemical analysis. The total content of allyl substituents from 5 to 50 per 100 chitosan units as a function of the component ratio in the reactive mixtures was revealed. Carrying out the reaction without any additives leads to the selective formation of N-alkylated derivatives, whereas in the presence of alkali the ethers of chitosan were preferentially formed. The results suggest that the proposed approach allows significantly higher yield of products to be obtained at high process speeds and significantly lower reagent consumption as compared with the liquid-phase synthesis in organic medium. The synthesized unsaturated derivatives are promising photosensitive components for use in laser stereolithography for fabrication of three-dimensional biocompatible structures with well-defined architectonics. |
format | Online Article Text |
id | pubmed-9066023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90660232022-05-04 Solvent-free synthesis and characterization of allyl chitosan derivatives Akopova, Tatiana A. Demina, Tatiana S. Cherkaev, Georgii V. Khavpachev, Mukhamed A. Bardakova, Kseniya N. Grachev, Andrey V. Vladimirov, Leonid V. Zelenetskii, Alexander N. Timashev, Petr S. RSC Adv Chemistry The solvent-free synthesis of allyl-substituted chitosan derivatives through reactive co-extrusion of chitosan powder with allyl bromide at shear deformation was performed. For the structural characterization, FTIR and NMR methods were employed. The results were confirmed by chemical analysis. The total content of allyl substituents from 5 to 50 per 100 chitosan units as a function of the component ratio in the reactive mixtures was revealed. Carrying out the reaction without any additives leads to the selective formation of N-alkylated derivatives, whereas in the presence of alkali the ethers of chitosan were preferentially formed. The results suggest that the proposed approach allows significantly higher yield of products to be obtained at high process speeds and significantly lower reagent consumption as compared with the liquid-phase synthesis in organic medium. The synthesized unsaturated derivatives are promising photosensitive components for use in laser stereolithography for fabrication of three-dimensional biocompatible structures with well-defined architectonics. The Royal Society of Chemistry 2019-07-04 /pmc/articles/PMC9066023/ /pubmed/35515576 http://dx.doi.org/10.1039/c9ra03830b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Akopova, Tatiana A. Demina, Tatiana S. Cherkaev, Georgii V. Khavpachev, Mukhamed A. Bardakova, Kseniya N. Grachev, Andrey V. Vladimirov, Leonid V. Zelenetskii, Alexander N. Timashev, Petr S. Solvent-free synthesis and characterization of allyl chitosan derivatives |
title | Solvent-free synthesis and characterization of allyl chitosan derivatives |
title_full | Solvent-free synthesis and characterization of allyl chitosan derivatives |
title_fullStr | Solvent-free synthesis and characterization of allyl chitosan derivatives |
title_full_unstemmed | Solvent-free synthesis and characterization of allyl chitosan derivatives |
title_short | Solvent-free synthesis and characterization of allyl chitosan derivatives |
title_sort | solvent-free synthesis and characterization of allyl chitosan derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066023/ https://www.ncbi.nlm.nih.gov/pubmed/35515576 http://dx.doi.org/10.1039/c9ra03830b |
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