Assignment of complex species by affinity capillary electrophoresis: The case of Th(IV)‐desferrioxamine B. Issue 21 (29th June 2020)

• Record Type: Journal Article
• Authors: Sladkov, Vladimir; Roques, Jérôme; Meyer, Michel
• Other Names: Lapizco‐Encinas Blanca guestEditor.; Wätzig Hermann guestEditor.
• Is Part Of: Electrophoresis. Volume 41:Issue 21/22(2020)
• Page Start: 1870
• Page End: 1877
• Publication Date: 2020-06-29
• Subjects: Affinity capillary electrophoresis -- Complexation -- Desferrioxamine B -- DFT -- Stability constants -- Thorium; Electrophoresis -- Periodicals; Electrophoresis -- Periodicals; 541.372
• DOI: 10.1002/elps.202000114
• Languages: English
• ISSNs: 0173-0835

Abstract

Abstract: The electrophoretic mobility change of desferrioxamine B (DFO) was monitored by UV absorption spectrophotometry upon increasing the thorium(IV) concentration in the background electrolyte at two acidities ([HClO4 ]Tot = 0.0316 and 0.0100 M). These data enabled to assess the speciation model and to determine the equilibrium constant of [Th(DFO)H2 ] 3+ at fixed ionic strength ( I = 0.1 M (H, Na)ClO4 ). Affinity capillary electrophoresis (ACE) turned out to be most helpful in identifying the complexed species by ascertaining its charge and protonation state. The assignment of the correct stoichiometry relied on the reliable estimation of the electrophoretic mobility by assuming similar hydrodynamic radii for (DFO)H4 + and the chelate. The value of the apparent equilibrium constant (log β 112 = 38.7 ± 0.4) obtained by ACE compares favorably well with those reported in the literature for thorium and a range of other metal ions, according to a linear free‐energy relationship. This method is useful for studying metal‐ligand binding equilibria and provides valuable information for further modelling the behavior of tetravalent actinides under environmental conditions. Structural information about the prevalent solution species in acidic conditions was gained by DFT calculations, confirming the bishydroxamato coordination mode of Th 4+ by the diprotonated ligand.