Related Experiment Video
Updated: Jul 26, 2026

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
Published on: August 19, 2013
Novel Colorimetric Anthracene-Based Thiosemicarbazone Probe for Selective Cyanide Ion Detection: From Synthesis to
Ashwathi Ayikkodan Veettil1, Sabeel Mohammed Basheer1
1Department of Chemistry, School of Advanced Sciences, VIT-AP University, Amaravati, Andhra Pradesh 522241, India.
Abstract:
A novel thiosemicarbazone, N'-(anthracen-9-ylmethylene) morpholine-4-carbothiohydrazide (MA), was synthesized and characterized for selective cyanide ion sensing. Interaction between the cyanide ion and sensor MA was examined thoroughly with the aid of absorption, emission, and 1H NMR spectra, and the binding constant was estimated. The detection limit obtained was much lower than those reported recently. The 1H NMR spectra titration studies clearly indicated that deprotonation occurs from the N-H group of the receptor. The sensing mechanism was further explored by density functional theory (DFT) and time-dependent DFT (TDDFT) methods using Gaussian16 software. In silico investigation reveals that the added cyanide ion abstracts a proton from the N-H group, which supports experimental results. The synthesized receptor MA was found to be a very good candidate for selective sensing of cyanide.
More Related Videos
Related Concept Videos
Measuring Reaction Rates
Gas Chromatography: Types of Detectors-II
High-Performance Liquid Chromatography: Types of Detectors

