Structural,spectroscopic and first‐principles studies of new aminocoumarin derivatives

The new aminocoumarin derivatives 3‐1‐(3‐hydroxyanilino)ethylidene]‐3H‐chromene‐2,4‐dione, ( 1 ), 3‐1‐(4‐hydroxyanilino)ethylidene]‐3H‐chromene‐2,4‐dione, ( 2 ), and 3‐1‐(2‐hydroxyanilino)ethylidene]‐3H‐chromene‐2,4‐dione, ( 3 ), all C₁₇H₁₃NO₄, were synthesized by reacting an equimolar amount of 3‐acetyl‐4‐hydroxycoumarin and the corresponding aminophenol in absolute ethanol. Structural and spectroscopic analysis of these phases revealed that derivatives ( 1 ) and ( 2 ) are isomers of previously reported ( 3 ) Brahmia et al. (2013). Acta Cryst. E 69 , o1296]. The crystal structures of meta derivative ( 1 ) and para derivative ( 2 ) were ab initio determined from powder X‐ray diffraction data using the direct‐space approach. Both ( 1 ) and ( 2 ) adopt the orthorhombic space group P2₁2₁2₁. These isomers show hydrogen bonds and rich π–π stacking, together with π…H interactions, which are built by conjugated systems of coumarin and phenol rings. In the crystalline lattice, the packing of ( 1 ) and ( 3 ) are mainly stabilized through O—H…O hydrogen bonding between neighbouring coumarin molecules, while hydrogen bonds between coumarin and water molecules build the stable crystal structure of derivative ( 2 ). A big similarity in the skeletons of the IR spectra of these isomers was noticed. Derivative ( 2 ) exhibits two weak bands which were not present in the spectra of the other two derivatives, at 2370 and 2948 cm^?1, which can be assigned to the O—H vibrations of the solvent (H₂O) trapped in the structure of ( 2 ). These aminocoumarin derivatives display absorption maxima in the visible region, attributed to π–π delocalization involving the whole electronic system of the compounds with a considerable charge‐transfer character originating from the aminophenyl ring and pointing towards the coumarin system which is characterized by a high electron‐accepting character. Additionally, the isolated molecular ground‐state geometries were optimized at the PBE0/TZP level and the electronic properties, molecular electrostatic potential and Hirshfeld charges were determined.