Naked-eye detection of F− and AcO− ions by Schiff base receptor

A Schiff base 2, composed with o-phenylenediamine and 5-nitro-salicylaldehyde have been synthesized as an anion receptor. It consists with conjugated imine, phenolic –OH and electron withdrawing substituent nitro (–NO2) group. Receptor 2 can recognize selectively biologically important F− and AcO− ions. The recognition properties have been investigated by naked-eye color change (colorless to yellow), followed by UV–vis spectral changes. Predicted stoichiometries of the complexes between receptor 2 and anions based on density functional theory (DFT) level calculations, corroborates well with experimental findings.

A Schiff base N,N′-bis(5-nitro-salicylidene)-1,2-phenylenediamine (2) can recognized biologically important F− and AcO− ion. The recognition properties have been investigated by naked-eye color change (colorless to yellow), followed by UV–vis spectral changes. Predicted stoichiometry of the complexes between 2 and anions based on density functional theory (DFT) level calculations corroborate well with experimental results.Figure optionsDownload as PowerPoint slideHighlights
► Schiff base can selectively detect F− and AcO− ions.
► Color change of the Schiff base in presence of anions were detected by naked-eye.
► Predicted complexation behavior from theoretical structural optimization corroborate with the experimental results.