Polymer complexes: XLX. Novel supramolecular coordination modes of structure and bonding in polymeric hydrazone sulphadrugs uranyl complexes

Novel five binuclear polymeric dioxouranium(VI) of azosulphadrugs (azodrug substances) azobenzene sulphonamides] were prepared for the first time. The infrared spectra of the samples were recorded and their fundamental vibration wave number was obtained. The resulting polymeric uranyl complexes were characterized on the basis of their elemental analyses, conductance and spectral (IR, NMR, and electronic spectra) data. The ligation modes of the azosulphadrugs ligands towards uranyl(II) ions were critically assigned and addressed properly on the basis of their IR and their uranyl(II) complexes. The theoretical aspects are described in terms of the well-known theory of 5d–4f transitions. The coordination geometries and electronic structures are determined from a framework for the modeling of novel polymer complexes. The values of ν₃ of the prepared complexes containing UO₂²⁺ were successfully used to calculate the force constant, F_UO (1n 10^?8 N/Å) and the bond length R_UO of the U–O bond. Wilson's, matrix method, Badger's formula, and Jones and El-Sonbati equations were used to calculate the U–O bond distances from the values of the stretching and interaction force constants. The most probable correlations between U–O force constant to U–O bond distance were satisfactorily discussed in terms of “Badger's rule”, “Jones” and “El-Sonbati equations”.