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Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer

A water soluble azo dye modified β-cyclodextrin polymer 4 was synthesized and used as a chemosensor for the detection of chlorinated phenols, model chlorinated by-products (CBPs) of water treatment for drinking purposes. The characterization of the intermediates and the azo dye modified β-CD polymer...

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Autores principales: Ncube, Phendukani, Krause, Rui W., Mamba, Bhekie B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3231385/
https://www.ncbi.nlm.nih.gov/pubmed/22163864
http://dx.doi.org/10.3390/s110504598
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author Ncube, Phendukani
Krause, Rui W.
Mamba, Bhekie B.
author_facet Ncube, Phendukani
Krause, Rui W.
Mamba, Bhekie B.
author_sort Ncube, Phendukani
collection PubMed
description A water soluble azo dye modified β-cyclodextrin polymer 4 was synthesized and used as a chemosensor for the detection of chlorinated phenols, model chlorinated by-products (CBPs) of water treatment for drinking purposes. The characterization of the intermediates and the azo dye modified β-CD polymer was done by UV/Vis Spectrophotometry, FT-IR and (1)H-NMR spectroscopies. The chlorophenols were capable of quenching the fluorescence of the polymer. The polymer showed greater sensitivity towards 2,4-dichlorophenol, with a sensitivity factor of 0.35 compared to 0.05 and 0.12 for phenol and 4-chlorophenol, respectively. The stability constants (K(s)) of the pollutants were also determined by the Benesi-Hildebrand method to be 2.104 × 10(3) M(−1) for 2,4-dichlorophenol and 1.120 × 10(2) M(−1) for 4-chlorophenol.
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spelling pubmed-32313852011-12-07 Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer Ncube, Phendukani Krause, Rui W. Mamba, Bhekie B. Sensors (Basel) Article A water soluble azo dye modified β-cyclodextrin polymer 4 was synthesized and used as a chemosensor for the detection of chlorinated phenols, model chlorinated by-products (CBPs) of water treatment for drinking purposes. The characterization of the intermediates and the azo dye modified β-CD polymer was done by UV/Vis Spectrophotometry, FT-IR and (1)H-NMR spectroscopies. The chlorophenols were capable of quenching the fluorescence of the polymer. The polymer showed greater sensitivity towards 2,4-dichlorophenol, with a sensitivity factor of 0.35 compared to 0.05 and 0.12 for phenol and 4-chlorophenol, respectively. The stability constants (K(s)) of the pollutants were also determined by the Benesi-Hildebrand method to be 2.104 × 10(3) M(−1) for 2,4-dichlorophenol and 1.120 × 10(2) M(−1) for 4-chlorophenol. Molecular Diversity Preservation International (MDPI) 2011-04-27 /pmc/articles/PMC3231385/ /pubmed/22163864 http://dx.doi.org/10.3390/s110504598 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Ncube, Phendukani
Krause, Rui W.
Mamba, Bhekie B.
Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title_full Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title_fullStr Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title_full_unstemmed Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title_short Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer
title_sort fluorescent sensing of chlorophenols in water using an azo dye modified β-cyclodextrin polymer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3231385/
https://www.ncbi.nlm.nih.gov/pubmed/22163864
http://dx.doi.org/10.3390/s110504598
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