Phosphoramides bearing isoxazole derivative: spectroscopic and structural characterization, study of hydrogen-bonding interactions and two lanthanide complexes (Ln~(III) = Ce and Eu)

摘要

In this study, the synthesis and spectroscopic characterization of new phosphoramides based on 3-amino-5-methylisoxazole with the formula R_2P(O)[NH–C_4H_4NO], R = C_6H_5O (1), C_6H_5 (2), RP(O)[NH-C_4H_4NO]_2, R = C_6H_5O (3), CH_3-C_6H_4O (4), C_6H_5NH (5), (C_6H_5)ClP(O)[NH–C_4H_4NO] (6) and two lanthanide complexes [Ln(2)_2(NO_3)_3(EtOH)]·EtOH, Ln~(III) = Ce (7) and Eu (8), have been reported. The structural study of (3) shows the presence of two conformers (crystallographically independent molecules) in the crystalline lattice, caused by different orientations of the phenyl and isoxazole rings. For (3), the intermolecular interactions have been studied by Hirshfeld surface analysis and fingerprint plots. Furthermore, the electronic and energy aspects of hydrogen bonds between molecules of (3) have been explored by density functional theory (DFT) calculations. X-ray crystallography of complexes (7) and (8) reveals that two phosphoramide ligands take part in coordination to the metal, one as monodentate from O_(phosphoryl), and the other one as chelate through O_(phosphoryl) and N_(ring). The complexes are also composed of two conformers in the solid-state structure. Quantum theory of atoms in molecules (QTAIM) analysis discloses the electrostatic nature of the Ln–ligand interaction.