Molecular Structure, Spectroscopic Assessment, PDOS, Topology Evaluation and Docking Studies of 2-Chloro-5-nitrobenzophenone

Abstract

The vibrational, electronic properties of 2-chloro-5-nitrobenzophenone (2C5NB) are explored experimentally, and theoretically (DFT) using B3LYP functional with LanL2DZ basis set. This has been performed for assignment vibrational frequencies that conjointly involves inserting beneficial evidence concerning the structure of the chosen compound. Based on PED, a comprehensive clarification of the FT-Infrared and FT-Raman spectra of the designated molecule were documented, with these studies agreeing satisfactorily with the experimental data. By mapping the total electron density isosurface with MEP, and contour map, charge density distribution and chemical reactivity spot of the 2C5NB were studied. Molecule stability ascending from hyper conjugative interactions and charge delocalization were explored using NBO analysis. For energies, the HOMO-LUMO diagram has been depicted. The transitions of the compound expression is (n→π*) in the UV-Vis region. The chemical changes of the molecule in 1H and 13C nuclear magnetic resonance were measured using the Gauge-Independent Atomic Orbital (GIAO) method and analysed using 1H and 13C NMR spectra. The non-zero value of μ and elevated β worth specify that the 2C5NB might be a good candidate for NLO content. In order to explore the simultaneous correlations of the different bonds of the 2C5NB, the total and partial DOS spectrum were intricated. Fukui functions were made to treasure the reactive site all over the molecule. The thermodynamic properties have been accomplished. The docking of molecule studies disclosed that the 2C5NB molecule performances a central role in binding proteins that inhibit L-glutamate oxidase. Minimum binding energy and intermolecular energy is perceived in the interaction.