Crystallographic, vibrational and theoretical studies of 2,3-diaminopyridinium selenate

Abstract

The new organic–inorganic salt, 2,3-diaminopyridinium selenate, has been synthesized and characterized by means of single-crystal X-ray crystallography, FT-IR and FT-Raman spectroscopy. A diprotonated organic ligand, H 2 1,3L 2+, existing in the crystal structure was theoretically shown to be the most stable cationic species of 2,3-diaminopyridine. The weak non-covalent forces of N–H⋯O type between the hydrogen atoms of the amino and ammonio groups of 2,3-diaminopyridinium cation and oxygen atoms of tetrahedral selenate anions determine three-dimensional arrangement with complex network of intermolecular interactions of hydrogen bond type (donor–acceptor distances from 2.697(3) Å to 3.088(3) Å). Vibrational spectra have been discussed in comparison with X-ray results. Juxtaposition of spectra of the complex with the pure organic ligand and deuterated analogue of the title compound allowed to give reliable assignments of most observed vibrational bands. Presented data can be useful in elucidation of molecular mechanism of uptake of tetrahedral SeO 4 2− anion by the living organisms.