Fluorescent “Turn-Off” Detection of Fluoride and Cyanide Ions Using Zwitterionic Spirocyclic Meisenheimer Compounds
Marina Benet,
Marc Villabona,
Carles Llavina,
Silvia Mena,
Jordi Hernando,
Rabih O. Al-Kaysi,
Gonzalo Guirado
Affiliations
Marina Benet
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
Marc Villabona
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
Carles Llavina
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
Silvia Mena
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
Jordi Hernando
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
Rabih O. Al-Kaysi
College of Science and Health Professions-3124, King Saud bin Abdulaziz University for Health Sciences/King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, 11426 Riyadh, Saudi Arabia
Gonzalo Guirado
Departament de Química, Universitat Autònoma de Barcelona, E-08193 Bellaterra, 08193 Barcelona, Spain
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−, NO2−, NO3−, or H2PO4−. These compounds can therefore be utilized as practical colorimetric and fluorescent probes for monitoring the presence of F− or CN− anions.