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Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
Published on: August 19, 2013
Anion-binding-induced and reduced fluorescence emission (ABIFE & ABRFE): A fluorescent chemo sensor for selective
Kumaresan Murugesan1, Vanthana Jeyasingh1, Sudha Lakshminarayanan1
1Department of Chemistry, International Research Centre, Centre for Supramolecular Chemistry, Kalasalingam Academy of Research and Education (KARE), Anand Nagar, Krishnankoil, Srivilliputtur, Tamil Nadu 626 126, India.
Abstract:
A new hydrazine based π-hole assisted, electron deficient turn-on/off fluorescent and colorimetric sensor L with anion-binding induced/reduced fluorescent emission (ABIFE & ABRFE) has been designed and synthesized. The prepared sensor L exhibited excellent turn-on fluorescence emission in the presence of cyanide ion through ABIFE. On the other hand, the receptor L turns-off its fluorescence intensity upon binding with fluoride; however, the reduced emission intensity of this complex of L is recovered by addition of cyanide. The sensor L is almost intact with other tested anions. To the best of our knowledge, this is the first report on sensing of cyanide and fluoride by a neutral hydrazine based receptor via anion-binding-induced fluorescence emission (ABIFE) and anion-binding-reduced fluorescence emission (ABRFE) mechanisms respectively. The observed ABIFE and ABRFE phenomena of L with cyanide is further supported by UV-Vis, Emission, 1H NMR and IR spectroscopic studies.
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