Quantum Chemical Study of the Water Exchange Mechanism of the Neptunyl(VI) and -(V) Aqua Ions.

The water exchange reaction of the neptunyl(VI) and -(V) aqua ions was investigated with quantum chemical methods. Associative ( a) and dissociative ( d) exchange mechanisms were studied. The geometries and vibrational frequencies were computed with density functional theory (DFT) and multiconfiguration self-consistent field (MCSCF) methods. The Gibbs activation energies (Δ G‡) for a and d pathways were calculated with DFT and wave function theory (WFT), extended general multiconfiguration quasi-degenerate second-order perturbation theory (XGMC-QDPT2) including spin-orbit (SO) coupling at the SO configuration interaction (CI) level. The DFT-WFT agreement for Δ G‡ was poor for the investigated functionals except for LC-BOP-LRD. Due to ligand-field effects, Δ G‡ for the associatively activated exchange reaction of NpO2(OH2)52+ with a fδ1 electron configuration is higher than for the actinyl(VI) aqua ions of U, Pu, and Am exhibiting f0, fδ2, and fδ2fϕ1 electron configurations.