DEHP - extractant binding to trivalent lanthanide Er 3+ : Fast binding accompanied by concerted angular motions of hydration water.
| Autor: | Liang Z; Department of Physics, University of Illinois at Chicago, 845 W. Taylor St., Chicago, Illinois 60607, USA., Vo T; Department of Physics, University of Illinois at Chicago, 845 W. Taylor St., Chicago, Illinois 60607, USA., Schweighofer KJ; Department of Chemistry and Biochemistry, University of California at Santa Cruz, Santa Cruz, California 95064, USA., Benjamin I; Department of Chemistry and Biochemistry, University of California at Santa Cruz, Santa Cruz, California 95064, USA., Schlossman ML; Department of Physics, University of Illinois at Chicago, 845 W. Taylor St., Chicago, Illinois 60607, USA. |
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| Jazyk: | angličtina |
| Zdroj: | The Journal of chemical physics [J Chem Phys] 2023 Apr 07; Vol. 158 (13), pp. 134715. |
| DOI: | 10.1063/5.0138019 |
| Abstrakt: | Solvent extraction of trivalent rare earth metal ions by organophosphorus extractants proceeds via binding of phosphoric acid headgroups to the metal ion. Water molecules in the tightly bound first hydration shell of the metal ions must be displaced by oxygen atoms from phosphoric acid headgroups. Here, we use classical molecular dynamics simulations to explore the event in which a fully hydrated Er 3+ binds to its first phosphoric acid headgroup. Approach of the headgroup into the region between the first and second hydration shells leads to a fast ejection of a water molecule that is accompanied by reordering of the hydration water molecules, including discretization of their angular positions and collective rotation about the metal ion. The water molecule ejected from the first shell is located diametrically opposite from the binding oxygen. Headgroup binding places a headgroup oxygen closer to Er 3+ than its first hydration shell and creates a loosely bound water that subsequently exchanges between the first shell and its environment. This second exchange of water also occurs at discrete angular positions. This geometrical aspect of binding may be of relevance to understanding the binding and transport of ion-extractant complexes that are expected to occur at the organic-aqueous liquid-liquid interface used in solvent extraction processes. |
| Databáze: | MEDLINE |
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