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A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative

The performance of a chemosensor is closely related to its structure. A new Schiff bass (DFSB) based on 4,5-diazafluorene units has been synthesized in this work. The interaction of DFSB with different metal ions has been studied using UV-vis absorption spectra and fluorescent spectra. The results s...

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Detalles Bibliográficos
Autores principales: Li, Hui, Wang, Jianzhi, Zhang, ShuJiang, Gong, ChenLiang, Wang, Feng
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/PMC9085904/
https://www.ncbi.nlm.nih.gov/pubmed/35547517
http://dx.doi.org/10.1039/c8ra05280h
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author Li, Hui
Wang, Jianzhi
Zhang, ShuJiang
Gong, ChenLiang
Wang, Feng
author_facet Li, Hui
Wang, Jianzhi
Zhang, ShuJiang
Gong, ChenLiang
Wang, Feng
author_sort Li, Hui
collection PubMed
description The performance of a chemosensor is closely related to its structure. A new Schiff bass (DFSB) based on 4,5-diazafluorene units has been synthesized in this work. The interaction of DFSB with different metal ions has been studied using UV-vis absorption spectra and fluorescent spectra. The results show that DFSB is a highly selective and sensitive probe for Al(3+) ions over other commonly coexisting metal ions in ethanol. A very obvious fluorescence enhancement effect was observed, and a turn-on ratio over 1312-fold was triggered with the addition of 10 equiv. of Al(3+) ions. What is more, such fluorescent responses could be detected by the naked eye under a UV-lamp. The lowest detection limit for Al(3+) was determined as 3.7 × 10(−8) M. The complex solution (DFSB–Al(3+)) exhibited reversibility with EDTA. These results may be caused by the unique molecular structure.
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spelling pubmed-90859042022-05-10 A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative Li, Hui Wang, Jianzhi Zhang, ShuJiang Gong, ChenLiang Wang, Feng RSC Adv Chemistry The performance of a chemosensor is closely related to its structure. A new Schiff bass (DFSB) based on 4,5-diazafluorene units has been synthesized in this work. The interaction of DFSB with different metal ions has been studied using UV-vis absorption spectra and fluorescent spectra. The results show that DFSB is a highly selective and sensitive probe for Al(3+) ions over other commonly coexisting metal ions in ethanol. A very obvious fluorescence enhancement effect was observed, and a turn-on ratio over 1312-fold was triggered with the addition of 10 equiv. of Al(3+) ions. What is more, such fluorescent responses could be detected by the naked eye under a UV-lamp. The lowest detection limit for Al(3+) was determined as 3.7 × 10(−8) M. The complex solution (DFSB–Al(3+)) exhibited reversibility with EDTA. These results may be caused by the unique molecular structure. The Royal Society of Chemistry 2018-09-12 /pmc/articles/PMC9085904/ /pubmed/35547517 http://dx.doi.org/10.1039/c8ra05280h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Hui
Wang, Jianzhi
Zhang, ShuJiang
Gong, ChenLiang
Wang, Feng
A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title_full A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title_fullStr A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title_full_unstemmed A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title_short A novel off-on fluorescent chemosensor for Al(3+) derived from a 4,5-diazafluorene Schiff base derivative
title_sort novel off-on fluorescent chemosensor for al(3+) derived from a 4,5-diazafluorene schiff base derivative
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085904/
https://www.ncbi.nlm.nih.gov/pubmed/35547517
http://dx.doi.org/10.1039/c8ra05280h
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