4.5 Article

Density Functional Theory Guided Investigation of Ligand-Induced Neptunyl-Neptunyl Interactions

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume 26, Issue 14, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202200693

Keywords

actinyl-actinyl interaction; CCI; density functional calculations; neptunium; raman spectroscopy

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Actinyl-actinyl interactions, particularly in the form of T- or D-shape, are commonly observed for the pentavalent neptunyl cation (Np(V)O-2)(+). This study utilized Density Functional Theory (DFT) calculations and Raman spectroscopy to investigate the formation of D-shaped interactions in the presence of different carboxylate ligands. Results show that the addition of carboxylate ligands promotes the spontaneous formation of hydrated T- and D-shaped forms. Raman spectra of the Np(V) carboxylate solutions exhibit vibrational modes associated with D-shaped interactions, indicating a dynamic system.
Actinyl-actinyl interactions are particularly prevalent for the pentavalent neptunyl cation (Np(V)O-2)(+) where these interactions appear either as a T- or D-shape (diamond-shape). T-shaped interactions have been previously identified in high concentration Np(V) solutions containing simple anions (NO3-, ClO4-, Cl-) whereas D-shaped have only been isolated in the solid-state in the presence of carboxylate ligands. In this study, Density Functional Theory (DFT) calculations were paired with Raman spectroscopy to evaluate the formation of D-shaped interactions in the presence of aliphatic (R=H (formate), CH3 (acetate), CH2CH3 (propionate)) and aromatic (R=C6H5 (benzoate), C6H4OH (4-hydroxybenzoate), C5H4N (isonicotinate)) carboxylate ligands. DFT studies indicate that the Delta G to form hydrated T- and D-shaped forms are not spontaneous but become so with the addition of the carboxylate ligands. Raman spectra of the Np(V) carboxylate solutions contained vibrational modes associated with the D-shaped interactions, but spectral changes observed over time indicate a dynamic system. Crystallization experiments from the Np(V) carboxylate systems confirmed the presence of D-shaped dimers for the aromatic carboxylates, suggesting that the choice of the anion in solution favors actinyl-actinyl interactions even at low concentrations (<= 20 mM) of Np(V).

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