People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Lindoy, Leonard F.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (1/1 displayed)
Places of action
Organizations | Location | People |
---|
article
Anion selectivity in zwitterionic amide-funtionalised metal salt extractants
Abstract
Amide-functionalised salen ligands capable of extracting metal salts have been synthesised and characterised. Single-crystal X-ray structure determinations of complexes of NiSO<sub>4</sub>, [Ni(L)(SO<sub>4</sub>)], confirm that the ionophores are in a zwitterionic form with Ni<sup>-II</sup>bound in the deprotonated salen moiety and the SO<sub>4</sub><sup>2-</sup> ion associated with protonated pendant N'-amidopiperazine groups. Treatment of [<i>N'</i>(L)(SO<sub>4</sub>)] with base removes the protons from the pendant amido-amine group resulting in loss of the SO<sub>4</sub><sup>2-</sup> ion and formation of metal-only complexes of type [Ni(L-2H)], which have been characterized by single-crystal X-ray diffraction. Three of the ligands with solubilities suitable for solvent extraction studies show loading and stripping pH-profiles that are suitable for the recovery of CuSO<sub>4</sub> or CuCl<sub>2</sub> from industrial leach solutions. The copper-only complexes, [Cu(L-2H)], are selective for Cl<sup>-</sup> over SO<sub>4</sub><sup>2-</sup> in both solvent extraction and bulk liquid membrane transport experiments and were found to bind Cl<sup>-</sup> in two steps via the formation of a 1:1:1 [Cu(L-H)Cl] assembly, followed by a 1:1:2 [Cu(L)Cl-<sub>2</sub>] assembly as the pH of the aqueous phase is lowered. The anion transport selectivity was evaluated for a number of other mono-charged anions and interestingly the ligands were found to display a preference for the Br- ion. To probe the influence of the Hofmeister bias on the selectivity of anion complexation, single-phase potentiometric titration experiments were employed to investigate the binding of SO<sub>4</sub><sup>2-</sup> and Cl<sup>-</sup> by one of the copper only complexes, [Cu(L-2H)] in 95%/5% MeOH/water. Under these conditions selectivity was reversed (SO<sub>4</sub><sup>2-</sup> > Cl<sup>-</sup>) confirming that the Hofmeister bias, which reflects the relative hydration energies of the anions, dominates the selectivity of anion extraction from aqueous media into CHCl<sub>3</sub>.