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Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds

Stable zwitterionic spirocyclic Meisenheimer compounds were synthesized using a one-step reaction between picric acid and diisopropyl (ZW1) or dicyclohexyl (ZW3) carbodiimide. A solution of these compounds displays intense orange fluorescence upon UV or visible light excitation, which can be quenche...

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Autores principales: Benet, Marina, Villabona, Marc, Llavina, Carles, Mena, Silvia, Hernando, Jordi, Al-Kaysi, Rabih O., Guirado, Gonzalo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150180/
https://www.ncbi.nlm.nih.gov/pubmed/29077037
http://dx.doi.org/10.3390/molecules22111842
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author Benet, Marina
Villabona, Marc
Llavina, Carles
Mena, Silvia
Hernando, Jordi
Al-Kaysi, Rabih O.
Guirado, Gonzalo
author_facet Benet, Marina
Villabona, Marc
Llavina, Carles
Mena, Silvia
Hernando, Jordi
Al-Kaysi, Rabih O.
Guirado, Gonzalo
author_sort Benet, Marina
collection PubMed
description Stable zwitterionic spirocyclic Meisenheimer compounds were synthesized using a one-step reaction between picric acid and diisopropyl (ZW1) or dicyclohexyl (ZW3) carbodiimide. A solution of these compounds displays intense orange fluorescence upon UV or visible light excitation, which can be quenched or “turned-off” by adding a mole equivalent amount of F(−) or CN(−) ions in acetonitrile. Fluorescence is not quenched in the presence of other ions such as Cl(−), Br(−), I(−), NO(2)(−), NO(3)(−), or H(2)PO(4)(−). These compounds can therefore be utilized as practical colorimetric and fluorescent probes for monitoring the presence of F(−) or CN(−) anions.
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spelling pubmed-61501802018-11-13 Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds Benet, Marina Villabona, Marc Llavina, Carles Mena, Silvia Hernando, Jordi Al-Kaysi, Rabih O. Guirado, Gonzalo Molecules Article Stable zwitterionic spirocyclic Meisenheimer compounds were synthesized using a one-step reaction between picric acid and diisopropyl (ZW1) or dicyclohexyl (ZW3) carbodiimide. A solution of these compounds displays intense orange fluorescence upon UV or visible light excitation, which can be quenched or “turned-off” by adding a mole equivalent amount of F(−) or CN(−) ions in acetonitrile. Fluorescence is not quenched in the presence of other ions such as Cl(−), Br(−), I(−), NO(2)(−), NO(3)(−), or H(2)PO(4)(−). These compounds can therefore be utilized as practical colorimetric and fluorescent probes for monitoring the presence of F(−) or CN(−) anions. MDPI 2017-10-27 /pmc/articles/PMC6150180/ /pubmed/29077037 http://dx.doi.org/10.3390/molecules22111842 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Benet, Marina
Villabona, Marc
Llavina, Carles
Mena, Silvia
Hernando, Jordi
Al-Kaysi, Rabih O.
Guirado, Gonzalo
Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title_full Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title_fullStr Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title_full_unstemmed Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title_short Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
title_sort fluorescent “turn-off” detection of fluoride and cyanide ions using zwitterionic spirocyclic meisenheimer compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150180/
https://www.ncbi.nlm.nih.gov/pubmed/29077037
http://dx.doi.org/10.3390/molecules22111842
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