Vibrational spectra of the ortho-nitroanilinium cation in torsional space. Theoretical studies vs. experimental data of ortho-nitroanilinium chloride

摘要

Crystal structure of the ortho-nitroanilinium chloride, (HoNA)Cl, was re-determined by means of X-ray single crystal diffraction. Hydrogen atoms of the ammonio form intra- and intermolecular hydrogen bonds which are arranged in chain and ring patterns. The patterns are described by the mathematical relations of the elementary graph-set descriptors. Since the interactions have a weak nature, the interpretation of the vibrational spectra was carried out with the help of theoretical calculations of the spectra for the HoNA~+ ion. In order to properly assign experimental bands, theoretical spectra were calculated at the B3LYP/6-31G(d,p) level of theory for the geometry of global minimum of HoNA~+ ion as a reference and for the other conformations, including in-crystal geometry of the ion, changing the relative position of the ammonio and nitro groups. Overall, the 89 spectra were analyzed as a two-dimensional dependence of each of 45 normal modes of the HoNA~+ ion on two dihedral angles, dih(HNCC) and dih(ONCC). Additionally, calculations were done for the in-crystal conformation of the (HoNA)Cl_3~(2 -) anion. Great increase of frequency is observed for the v_7 (641 cm~(-1)), where the H1C atom is involved in, because the intramolecular N–H1C?··O hydrogen bond weakens upon rotation of the NH_3~+ group. PED analysis shows that also the modes of vibrations changes upon rotation. The mode of vibrations for the (HoNA)Cl_3~(2–) anion differs from the HoNA~+ ion, especially for the m(N–H) vibrations. Besides, when three chloride anions where included in the calculations, only then the experimental spectra were well reproduced.