Resumen de Crystal structure of (e)-n′-((1h-pyrrol-2-yl)methylene)-4-hydroxybenzohydrazide
Ghodrat Mahmoudi, Sadegh Rostamnia, Guillermo Zaragoza de Aguila, Iván Brito, Jonathan Cisterna, Alejandro Cárdenas
The title compound corresponds to an enaminone E isomer in the solid state. X-ray structure shows that this crystallizes in the orthorrombic system, with space group Pna21 with 2 independent molecules in the asymmetric unit in a non-centrosymmetric setting. The CNNC unit forms dihedral angles of 5.9(3)/2.1(3); 19.7(3)/17.6(3)° with the pyrrole and phenol rings for molecules A and B respectively. The main differences between both molecules is the dihedral torsion between rings, their mean planes form dihedral angles of 25.45(15) and 15.38(15)° for the molecules A and B. In the asymmetric unit, molecules are linked by two weak N – H⋯O hydrogen bonds with set graph-motif R 2 2(16). The crystal structure of title compound generates a two dimensional supramolecular network lying parallel (110) with hydrogen bonds interactions between O – H⋯O and N – H⋯O along to [100] and [001] direction with graph set motifs R 1 2(5), R 2 2(10), C 1 1(8) and C 1 1(12). π stacking interactions are not observed. Hirshfeld surface analysis were used to verify the contributions of the different intermolecular interactions. Both molecules are essentially overlaid between them with RMSD = 0.0574; max D = 0.1211 Å considering inversion and flexibility.
