Identification of supramolecular dimers in the crystal structure of (Z)-1-(((5-fluoropyridin-2-yl)amino)methylene)naphthalen-2(1H)-one via C(sp2)—H⋯F hydrogen bonding: A combined experimental and theoretical study

Abstract

Title compound C16H11FN2O (1) is nearly planar, and adopts the keto-amine form with a strong intramolecular N—H⋯O hydrogen bond. Interestingly, the compound features an intramole­cular C—H⋯N weak interaction in the crystal. In addition, the molecules of 1 form supra­molecular dimers via C—F⋯H—C13 weak interactions. The nature and energies of intermolecular noncovalent interactions, which are responsible for the supramolecular dimerization, are studied theoretically using DFT calculations, and the topological analysis of the electron density distribution is performed within the formalism of Bader's theory (QTAIM method).