Abstract

4-Dimethylaminopyridine-Picric acid (4DMAP:PA) co-crystals were synthesized by slow evaporation technique using C2H5OH as the solvent. The molecular structure has been characterized using spectroscopic and single crystal X-ray diffraction techniques. The molecule contains O–H…O, O–H…N, C–H…O and π…π interactions. The C12–H12…O4A and C12A–H12A…O4 forms a dimer with a R22(10) graph set motif. Few intermolecular C–H…O and O–H…N bonds result in the formation of a R22(9)ring motif. The structure has been theoretically optimized by using Hartree-Fock (HF) and density functional theory (DFT) approaches. The DFT calculation led to the investigation of FMO, MEP, Mulliken charges and HOMO – LUMO, energy gap. The Hirshfeld surface (HS) and fingerprint plots analysis provided an insight in the molecular shape and visual assessment of the intermolecular interactions in the crystal structure. The co-crystal suggests antifungal activity against the fungal pathogens when compared with the standard antifungal drug fluconazole.

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