Abstract
A novel schiff base derivative containing 1, 2, 4-triazole moiety (NBTMPA) has been synthesized from 4- [1, 2, 4] triazol-1-ylmethyl-phenylamine and 4-nitrobenzaldehyde in the presence of glacial acetic acid in an ethanolic medium. The absorbance and fluorescence spectra of (4-nitro-benzylidene)-(4- [1, 2, 4] triazol-1-ylmethyl-phenyl)-amine (NBTMPA) were recorded in various solvents to investigate their solvatochromic behaviour. Dipole moments of the two electronic states of NBTMPA were calculated from solvatochromic spectral shifts. These were correlated with the refractive index (n) and dielectric constant (ε) of various solvents. Theoretical calculations were performed to estimate the excited state dipole moment on the basis of different solvent correlation methods, like the Bilot–Kawski, Bakhshiev, Lippert–Mataga, Kawski–Chamma–Viallet and Reichardt methods. The dipole moment in the excited state was found to be higher than that in the ground state due to a substantial redistribution of electron densities and charges. Using a multiple regression analysis, the solvent–solute interactions were determined by means of Kamlet Taft parameters (α, β, π*). Computational studies were performed by Gaussian 09W software using a time-dependent density functional theory (TDDFT) in order to calculate the atomic charges and frontier molecular orbital energies in the solvent phase. The calculations indicated that the dipole moment of the molecule in an excited state is much higher than that in a ground state. The chemical stability of NBTMPA was determined by means of chemical hardness (η) using HOMO–LUMO energies. The reactive centres in the molecule were also identified by molecular electrostatic potential (MESP) 3D plots as a result of a TDDFT computational analysis.
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