Specific interaction between uranium anionic complexes and the cations of bis(trifluoromethylsulfonyl)imide based ionic liquids.

The redox properties of uranium(IV) hexachloro complex have been investigated with a glassy carbon electrode in four bis(trifluoromethylsulfonyl)imide (Tf2N(-)) based ionic liquids (ILs): the 1-butyl-3-methylimidazolium ([BuMeIm](+)), the 1-butyl-2,3-dimethylimidazolium ([BuMe2Im](+)), the N-butylmethylpyrrolidinium ([BuMePyr](+)), and the tributyl-methylammonium ([MeBu3N](+)). The cyclic voltammetric analysis has revealed two main redox systems: U(V)Cl6(-)/U(IV)Cl6(2-) around 0.2 V and U(IV)Cl6(2-)/U(III)Cl6(3-) around -2 V. The formation of U(V)Cl6(-), a non-dioxo uranium(V) species, can then be observed at the electrode in [Tf2N](-) based ILs. This work also provides evidence of a specific interaction between the uranium anionic species and the IL cations because the standard potentials of both redox couples depend on the IL. The interaction extent has been evaluated by comparison of the IL cation number associated with the uranium anionic complex. For that purpose, the standard potentials of both systems have been measured in the less interacting medium [MeBu3N][Tf2N] as a function of the [BuMeIm](+), [BuMe2Im](+), and [BuMePyr](+) concentration. Predominance diagrams for uranium hexachloro complexes, analogous to the Pourbaix diagram, have then been built in [MeBu3N][Tf2N] depending on the IL cations concentration. The exploitation of these diagrams leads to the conclusion that the interaction is function of the charge of the uranium hexachloro complex (U(V)Cl6(-) < U(IV)Cl6(2-) < U(III)Cl6(3-)) and the IL cation ([BuMe2Im](+) < [BuMePyr](+) < [BuMeIm](+)). The influence of the IL cation could be correlated to the size and the electropositivity of the IL cation. The association would occur by H-bonding and electrostatic interaction. Ab initio calculations were also carried out to evaluate the strength of the interaction between the anionic uranium(IV) chloro complex and the IL cations. The results show that [BuMeIm](+) interacts the most and [MeBu3N](+) the least with U(IV)Cl6(2-), and the magnitude of the interaction is comparable for [BuMe2Im](+) and [BuMePyr](+).

Thermodynamic study of the complexation of protactinium(V) with diethylenetriaminepentaacetic acid.

The complex formation of protactinium(V) with DTPA was studied at different temperatures (25-50 °C) and ionic strengths (0.1-1 M) with the element at tracer scale. Irrespective of the temperature and ionic strength studied, only one neutral complex with (1:1) stoichiometry was identified from solvent extraction and capillary electrophoresis coupled to ICP-MS (CE-ICP-MS) experiments. Density Functional Theory (DFT) calculations revealed that two complexes can be considered: Pa(DTPA) and PaO(H2DTPA). The associated formation constants were determined from solvent extraction data at different ionic strengths and temperatures and then extrapolated to zero ionic strength by SIT methodology. These constants are valid, regardless of complex form, Pa(DTPA) or PaO(H2DTPA). The standard thermodynamic data determined with these extrapolated constants revealed a very stable complex formed energetically by an endothermic contribution which is counter balanced by a strong entropic contribution. Both, the positive enthalpy and entropy energy terms suggest the formation of an inner sphere complex.

New insights into formation of trivalent actinides complexes with DTPA.

Complexation of trivalent actinides with DTPA (diethylenetriamine pentaacetic acid) was studied as a function of pcH and temperature in (Na,H)Cl medium of 0.1 M ionic strength. Formation constants of both complexes AnHDTPA(-) and AnDTPA(2-) (where An stands for Am, Cm, and Cf) were determined by TRLFS, CE-ICP-MS, spectrophotometry, and solvent extraction. The values of formation constants obtained from the different techniques are coherent and consistent with reinterpreted literature data, showing a higher stability of Cf complexes than Am and Cm complexes. The effect of temperature indicates that formation constants of protonated and nonprotonated complexes are exothermic with a high positive entropic contribution. DFT calculations were also performed on the An/DTPA system. Geometry optimizations were conducted on AnDTPA(2-) and AnHDTPA(-) considering all possible protonation sites. For both complexes, one and two water molecules in the first coordination sphere of curium were also considered. DFT calculations indicate that the lowest energy structures correspond to protonation on oxygen that is not involved in An-DTPA bonds and that the structures with two water molecules are not stable.

Thermodynamical and structural study of protactinium(V) oxalate complexes in solution.

The complexation of protactinium(V) by oxalate was studied by X-ray absorption spectroscopy (XAS), density functional theory (DFT) calculations, capillary electrophoresis coupled with inductively coupled plasma mass spectrometry (CE-ICP-MS) and solvent extraction. XAS measurements showed unambiguously the presence of a short single oxo-bond, and the deduced structure agrees with theoretical calculations. CE-ICP-MS results indicated the formation of a highly charged anionic complex. The formation constants of PaO(C(2)O(4))(+), PaO(C(2)O(4))(2)(-), and PaO(C(2)O(4))(3)(3-) were determined from solvent extraction data by using protactinium at tracer scale (C(Pa) < 10(-10) M). Complexation reactions of Pa(V) with oxalate were found to be exothermic with relatively high positive entropic variation.

Solvation of UCl6(2-) anionic complex by MeBu3N(+), BuMe2Im(+), and BuMeIm(+) cations.

The complexes [MeBu 3N] 2[UCl 6] and [BuMe 2Im] 2[UCl 6] were characterized in the solid state and in solution of [MeBu 3N][Tf 2N], [BuMe 2Im][Tf 2N], and [BuMeIm][Tf 2N] room-temperature ionic liquids using single-crystal XRD, EXAFS, electrochemistry, UV-visible absorption spectroscopy, and NMR. In the solid state and in solution, the existence of hydrogen bonding between the UCl 6 (2-) complex and the ionic liquid cations was revealed by these techniques. The MeBu 3N (+) cation interacts with UCl 6 (2-) via the protons on the alpha-carbon atoms of nitrogen. The protons of the imidazolium ring account for the interaction between the BuMe 2Im (+) cation and the UCl 6 (2-) anion. For the BuMeIm (+) cation the major interaction was confirmed between the most acidic proton on C(2) and the chlorides of UCl 6 (2-). The experimental results also show that the intensity of the interaction between the UCl 6 (2-) anion and the cation varies with the ionic liquid cation in the following order: MeBu 3N (+) approximately BuMe 2Im (+) << BuMeIm (+).

First structural characterization of a protactinium(V) single oxo bond in aqueous media.

The present work describes the first structural studies of protactinium(V) in sulfuric and hydrofluoric acid media using X-ray absorption spectroscopy. The results show unambiguously the absence of the trans-dioxo bond that characterizes the other early actinide elements such as U and Np. In concentrated sulfuric acid (13 M), Pa(V) is proved to exhibit a single oxo bond as postulated in the literature for species in more dilute media. In a 0.5 M HF medium, XANES and EXAFS spectra indicate the absence of any oxo bond: Pa(V) exists in the form of a pure fluoro complex.