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Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization
The copolymer of 3-hexylthiophene (3HT) and fluorene (F) was directly grafted onto chitin and chitosan using FeCl(3) as an oxidant. The properties of the grafted chitin/chitosan were characterized by Fourier transform infrared (FT-IR) spectroscopy, UV-Vis spectroscopy, fluorescence spectroscopy, X-r...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078334/ https://www.ncbi.nlm.nih.gov/pubmed/35540309 http://dx.doi.org/10.1039/c8ra00287h |
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author | Phung Hai, Thien An Sugimoto, Ryuichi |
author_facet | Phung Hai, Thien An Sugimoto, Ryuichi |
author_sort | Phung Hai, Thien An |
collection | PubMed |
description | The copolymer of 3-hexylthiophene (3HT) and fluorene (F) was directly grafted onto chitin and chitosan using FeCl(3) as an oxidant. The properties of the grafted chitin/chitosan were characterized by Fourier transform infrared (FT-IR) spectroscopy, UV-Vis spectroscopy, fluorescence spectroscopy, X-ray diffraction analysis, thermogravimetric analysis (TGA), transmission electron microscopy-energy dispersive X-ray spectroscopy, and quantum yield measurements. The UV-Vis absorption peaks of the chitin/chitosan grafted with 3-hexylthiophene and fluorene copolymer were increasingly blue-shifted upon increasing the fluorene content and the red-shifted emission of the grafted chitin/chitosan were controlled by varying the monomers feed of the 3HT/F units. The hypsochromic and bathochromic shifts of chitin/chitosan were ascribed to the (3HT/F) moieties grafted to their surface. The quantum yield of grafted chitin/chitosan increased upon increasing the fluorene content. The TGA and XRD analysis revealed that the thermal stability and crystallinity of chitin/chitosan decreased upon grafting the copolymer of fluorene and 3-hexylthiophene. This article represents a simple route towards the surface modification of chitin and chitosan using conducting copolymers, providing multicolor chitin and chitosan via a one-step reaction. |
format | Online Article Text |
id | pubmed-9078334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90783342022-05-09 Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization Phung Hai, Thien An Sugimoto, Ryuichi RSC Adv Chemistry The copolymer of 3-hexylthiophene (3HT) and fluorene (F) was directly grafted onto chitin and chitosan using FeCl(3) as an oxidant. The properties of the grafted chitin/chitosan were characterized by Fourier transform infrared (FT-IR) spectroscopy, UV-Vis spectroscopy, fluorescence spectroscopy, X-ray diffraction analysis, thermogravimetric analysis (TGA), transmission electron microscopy-energy dispersive X-ray spectroscopy, and quantum yield measurements. The UV-Vis absorption peaks of the chitin/chitosan grafted with 3-hexylthiophene and fluorene copolymer were increasingly blue-shifted upon increasing the fluorene content and the red-shifted emission of the grafted chitin/chitosan were controlled by varying the monomers feed of the 3HT/F units. The hypsochromic and bathochromic shifts of chitin/chitosan were ascribed to the (3HT/F) moieties grafted to their surface. The quantum yield of grafted chitin/chitosan increased upon increasing the fluorene content. The TGA and XRD analysis revealed that the thermal stability and crystallinity of chitin/chitosan decreased upon grafting the copolymer of fluorene and 3-hexylthiophene. This article represents a simple route towards the surface modification of chitin and chitosan using conducting copolymers, providing multicolor chitin and chitosan via a one-step reaction. The Royal Society of Chemistry 2018-02-13 /pmc/articles/PMC9078334/ /pubmed/35540309 http://dx.doi.org/10.1039/c8ra00287h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Phung Hai, Thien An Sugimoto, Ryuichi Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title | Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title_full | Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title_fullStr | Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title_full_unstemmed | Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title_short | Fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
title_sort | fluorescence control of chitin and chitosan fabricated via surface functionalization using direct oxidative polymerization |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078334/ https://www.ncbi.nlm.nih.gov/pubmed/35540309 http://dx.doi.org/10.1039/c8ra00287h |
work_keys_str_mv | AT phunghaithienan fluorescencecontrolofchitinandchitosanfabricatedviasurfacefunctionalizationusingdirectoxidativepolymerization AT sugimotoryuichi fluorescencecontrolofchitinandchitosanfabricatedviasurfacefunctionalizationusingdirectoxidativepolymerization |