Abstract
Investigation of ground state geometry, molecular properties and electronic structure of methyl 1H-indol-5-carboxylate has been reported for the first time using the implements of density functional theory. The two possible conformers of the title compound were first optimized at B3LYP/6-31G(d) and then further at B3LYP, M06-2X and CAM-B3LYP functionals at 6-311++G(d,p) basis set. A comprehensive vibrational analysis has been performed for both the conformers at B3LYP/6-311++G(d,p). Good agreement between theoretical spectral data with experimental spectra has been obtained. Polarizability and first static hyperpolarizability have been compared at different functionals used in the present study. To estimate the intra-molecular delocalization along with the inter-molecular interaction, the NBO analysis has been done for monomer and dimer of the title molecule. Topological parameters at the bond critical point involved in intermolecular hydrogen-bonding have also been calculated using AIM theory to assess the strength of hydrogen bonding. Effects of solvents (water, carbon tetrachloride and chloroform) on the optimized geometry and the inter-molecular hydrogen bonding have been evaluated. UV–Vis spectrum of the title compound was also recorded and electronic properties such as frontier orbitals and their corresponding energy gap have also been calculated by TD-DFT approach.
A combined experimental and theoretical DFT (B3LYP, CAM-B3LYP and M06-2X) study on electronic structure, hydrogen bonding, solvent effects and spectral features of Methyl 1H-indol-5-carboxylate. [Display omitted]
•Solvent effects and spectral features of C10H9NO2 at B3LYP, CAM-B3LYP and M06-2X.•NBO and topological analysis of the dimer to estimate intermolecular hydrogen bond strength.•B3LYP hyperpolarizability values are higher by 15% and 18% respectively to CAM-B3LYP and M06-2X values.