Molecular structure, electronic properties, spectroscopic, quantum computational studies of 1-(4-hydroxy-3-methoxyphenyl)ethanone-effective anticancer medicine

Abstract

The molecular structure of 1-(4-hydroxy-3-methoxyphenyl) ethenone has been optimized, and its various parameters were ascertained, using Density Functional Theory. The molecule’s Fourier Transform-Infra Red and Raman spectra are recorded and examined. By comparing the computational and experimental results, molecular structure, bond length, and vibrational band intensity were all interpreted. The Integral Equation Formalism polarizable continuum model’s depictions of electronic and Frontier Molecular Orbital solvent interaction investigations are sported to perceive the charge transfer among the atoms of the molecule in eco-green solvents such as water, acetone, and ethanol. The reactivity sites can be studied by locating and charting the electron density on the surface. The compound’s hardness, softness, electrophilicity, and ionization potential were all analyzed. The pharmacological effects and intra-molecular hyper conjugative interactions are liable for its molecular stability, as shown by Natural Bond Orbital research. Topological studies, including Electron Localized Function, Localized Orbital Locator, and Reduced density gradient analysis, were performed to locate the compound’s bonding area and Vander Waals interactions. Urea was used as a reference compound to examine the substance’s non-linear optical characteristics. Total Density of States has investigated the role of molecular orbitals. Drug-likeness, a Ramachandran plot, and molecular docking were also performed to further analyze 1-(4-hydroxy-3-methoxyphenyl) ethanone’s biological activity. The docking results lend credence to the idea that the title compound could function as a powerful cancer treatment.