Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Phung Hai, Thien An, Sugimoto, Ryuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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
_version_ 1784702307421650944
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