Relativistic theoretical studies on hydrogen bonds and the electronic structure of aqueous solvated bis(uranyl) complex: An insight into explicit and/or implicit solvent effects

To understand the chemical behavior of uranyl complexes in water, a bis-uranyl [(phen)(UO)(μ-F)(F)] (A; phen = phenanthroline, μ = doubly bridged) and its hydrated form A · (HO) (n = 2, 4 and 6) were examined using scalar relativistic density functional theory. The addition of water caused the phen ligands to deviate slightly from the U(μ-F) plane, and red-shifts the U-F-terminal and U = O stretching vibrations. Four types of hydrogen bonds are present in the optimized hydrated A · (HO) complexes; their energies were calculated to fall within the range 4.37-6.77 kcal mol, comparable to the typical values of 5.0 kcal mol reported for hydrogen bonds. An aqueous environment simulated by explicit and/or implicit models lowers and re-arranges the orbitals of the bis-uranyl complex. [Figure not available: see fulltext.] © 2013 Springer-Verlag Berlin Heidelberg.