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Issue 11, 2011
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Synthesis and evaluation of novel water-soluble ligands for the complexation of metals during the partitioning of actinides

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Abstract

Different types of water-soluble ligands were synthesized and their capability was evaluated by solvent extraction studies to complex trivalent actinides and suppress their extraction by a strong lipophilic ligand, such as TODGA. The back extraction efficiency of hydrophilic diglycolamide (DGA) derivatives with a varying number of ethylene glycol groups, or containing sodium acetate moieties on the amidic nitrogen shows a decrease in back-extraction efficiency with increasing number of ethylene glycol units on the amidic nitrogen at various pH values of the aqueous phase. Among the P[double bond, length as m-dash]S donating ligands only the ligand with a malonamide backbone exhibits a high reverse extraction efficiency, although, with no selectivity for americium. Within the water-soluble tripodal ligands, i.e. the amide derivatives of nitrilotriacid with N,N-dimethyl and N,N-bis(hydroxyethyl) moieties, the first one shows a pronounced selectivity for Am(III) over Eu(III), with a maximum separation factor of 11.1, while the latter one more efficiently complexes the radionuclides in the aqueous phase with a maximum separation factor of 5. Isothermal microcalorimetry experiments of the complexation of Eu(III) by a selected series of ligands confirm the observed trend in the back extraction properties.

Graphical abstract: Synthesis and evaluation of novel water-soluble ligands for the complexation of metals during the partitioning of actinides

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Publication details

The article was received on 14 Jun 2011, accepted on 04 Aug 2011 and first published on 06 Sep 2011


Article type: Paper
DOI: 10.1039/C1NJ20523D
Citation: New J. Chem., 2011,35, 2591-2600
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    Synthesis and evaluation of novel water-soluble ligands for the complexation of metals during the partitioning of actinides

    M. Iqbal, J. Huskens, M. Sypula, G. Modolo and W. Verboom, New J. Chem., 2011, 35, 2591
    DOI: 10.1039/C1NJ20523D

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