Acylthiourea derivatives as colorimetric sensors for anions: Synthesis, characterization and spectral behaviors

Spectrochim Acta A Mol Biomol Spectrosc. 2016 Jan 15:153:471-7. doi: 10.1016/j.saa.2015.09.003. Epub 2015 Sep 8.

Abstract

Several acylthioureas have been synthesized to develop colorimetric sensors for detection of biologically important anions. UV-vis titration experiments indicated that the absorbance values have a good linear relationship with concentration of anions when the anions were added in AR-1, AR-4 and AR-6 sensor molecules. The detection limit to AcO(-) and F(-) is 5×10(-6) mol/L when the concentration of receptors are 2×10(-5) mol/L. Especially, compounds AR-1 and AR-4, decorated with strong electron-withdrawing NO2 substituent, showed augmented anion sensing properties, being capable of naked-eye detecting of F(-) and AcO(-) when the water content is lower than 15%. The recognition details of anion sensing were also assessed using (1)H NMR technique and confirmed that the basic anions induced deprotonation of N-H.

Keywords: Acylthiourea; Anion recognition; Colorimetric sensor; Naked-eye detection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anions / analysis*
  • Color
  • Colorimetry / instrumentation*
  • Colorimetry / methods*
  • Limit of Detection
  • Proton Magnetic Resonance Spectroscopy
  • Spectrophotometry, Infrared
  • Spectrophotometry, Ultraviolet
  • Thiourea / chemical synthesis*
  • Thiourea / chemistry*
  • Water / chemistry

Substances

  • Anions
  • Water
  • Thiourea