Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2007Anion selectivity in zwitterionic amide-funtionalised metal salt extractants31citations

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Chart of shared publication
Plieger, Paul G.
1 / 1 shared
Collinson, Simon R.
1 / 2 shared
Blake, Alexander J.
1 / 11 shared
Tasker, Peter A.
1 / 3 shared
Galbraith, Stuart G.
1 / 1 shared
Li, Li
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Schröder, Martin
1 / 10 shared
Wang, Qiang
1 / 2 shared
Wilson, Claire
1 / 15 shared
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2007

Co-Authors (by relevance)

  • Plieger, Paul G.
  • Collinson, Simon R.
  • Blake, Alexander J.
  • Tasker, Peter A.
  • Galbraith, Stuart G.
  • Li, Li
  • Schröder, Martin
  • Wang, Qiang
  • Wilson, Claire
OrganizationsLocationPeople

article

Anion selectivity in zwitterionic amide-funtionalised metal salt extractants

  • Plieger, Paul G.
  • Lindoy, Leonard F.
  • Collinson, Simon R.
  • Blake, Alexander J.
  • Tasker, Peter A.
  • Galbraith, Stuart G.
  • Li, Li
  • Schröder, Martin
  • Wang, Qiang
  • Wilson, Claire
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>.

Topics
  • impedance spectroscopy
  • phase
  • x-ray diffraction
  • experiment
  • copper
  • amine
  • solvent extraction
  • titration