2-Aminophenols based Schiff bases as fluorescent probes for selective detection of cyanide and aluminium ions - Effect of substituents

Three Schiff base based probes are designed and synthesized by facile condensation of a commercially available fluorophore 2,6-diformyl-4-tert-butylphenol with 4-nitro-2-aminophenol (KP1), 2-aminophenol (KP2) and 4-tert-butyl-2-aminophenol (KP3) and are characterized using various spectral techniques. The probes exhibit high selectivity and sensitivity CN and Al(III) ions with striking fluorescent signaling responses in H2O-DMSO (1:1, v/v) medium. The mechanism of the probes' detection of CN involves deprotonation of the phenolic -OH group(s) followed by nucleophilic addition of CN onto imine C-atom. The H-1 NMR chemical shifts of the -OH protons of 2-aminophenol moiety exhibits a linear correlation with the Hammett's substituent constants (sigma(p)), yielding a positive reaction constant (rho). In KP1, the electron-withdrawing nitro substituent polarizes the imine bond to a larger extent than in KP2, resulting in easier addition of CN to imine C-atom. The electron releasing tert-Bu substituent in KP3 produces the opposite effect leading to a sluggish addition reaction. The separately populated HOMO and LUMO in 101 and a relatively lower HOMO-LUMO energy gap indicate substantial intramolecular charge transfer (ICT) character, leading to weak fluorescence emission. The large reduction in HOMO-LUMO energy gap, in KP1, upon addition of cyanide is responsible for the greater enhancement in fluorescence with blue shift upon addition of CN . Formation of tetrahedral Probe-Al(III) complex prevents the isomerization of imine bond, leading to enhancement in fluorescence and contribution from chelation enhanced fluorescence. As these probes show very low limits of detection of these ions, their practical utility has also been demonstrated. (C) 2020 Elsevier B.V. All rights reserved.

Automated summary

Three Schiff base based probes with high selectivity and sensitivity towards CN and Al(III) ions have been designed and synthesized, exhibiting remarkable fluorescent signaling responses in H2O-DMSO medium. The detection mechanism involves deprotonation and nucleophilic addition, characterized by various spectral techniques. The probes' practical utility has been demonstrated due to their low limits of detection for these ions.