Ion association with tetra-n-alkylammonium cations stabilizes higher-oxidation-state neptunium dioxocations.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30610189.
- Also identified by DOI 10.1038/s41467-018-07982-5 and PMC identifier 6320366.
- Licence recorded as CC BY.
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Abstract
Extended-coordination sphere interactions between dissolved metals and other ions, including electrolyte cations, are not known to perturb the electrochemical behavior of metal cations in water. Herein, we report the stabilization of higher-oxidation-state Np dioxocations in aqueous chloride solutions by hydrophobic tetra-n-alkylammonium (TAA<sup>+</sup>) cations-an effect not exerted by fully hydrated Li<sup>+</sup> cations under similar conditions. Experimental and molecular dynamics simulation results indicate that TAA<sup>+</sup> cations not only drive enhanced coordination of anionic Cl<sup>-</sup> ligands to Np<sup>V/VI</sup> but also associate with the resulting Np complexes via non-covalent interactions, which together decrease the electrode potential of the Np<sup>VI</sup>/Np<sup>V</sup> couple by up to 220 mV (ΔΔG = -22.2 kJ mol<sup>-1</sup>). Understanding the solvation-dependent interplay between electrolyte cations and metal-oxo species opens an avenue for controlling the formation and redox properties of metal complexes in solution. It also provides valuable mechanistic insights into actinide separation processes that widely use quaternary ammonium cations as extractants or in room temperature ionic liquids.