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The complexation of selected trivalent lanthanide ions with derivatives of the tetranitrogen donor ligands 6,6′-bis-1R,1 H -1,2,3-triazol-4-yl-2,2′-bipyridines (BTzBPs, R = alkyl or aryl) was investigated in solid state and in solution. An anhydrous solid [Ce(Bn-BTzBP)(NO 3 ) 3 ] (Bn = benzene) complex was synthesized and characterized by single-crystal X-ray diffraction. Eu(III) complexes with the 2-ethyl(hexyl) derivative EH-BTzBP in methanol were studied by time-resolved fluorescence spectroscopy. Earlier studies have identified the EH-BTzBP as a potentially useful solvent extraction reagent for the separation of americium from lanthanide metal ions, a challenging component of advanced nuclear fuel cycles for actinide transmutation. To help identify species formed in the extraction process, the influence of 2-bromohexanoic acid (identified as an essential component of the separation system) on Eu(III) complexes was investigated. Comparison with an organic phase after extraction of Eu(III) by EH-BTzBP and 2-bromohexanoic acid showed that both 1:1 and 1:2 (Eu/EH-BTzBP) complexes are involved in the extraction. UV–visible spectrophotometry was used to compare Eu(III) stability constants with those of other Ln(III) complexes.
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Muller et al. (2016) studied this question.
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