Extraction and complexation studies with 2,6-bis(5-(tert-butyl)-1H-pyrazol-3-yl)pyridine in the presence of 2-bromohexanoic acid

被引:1
|
作者
Stracke, Jonas [1 ,2 ]
Wessling, Patrik [2 ]
Sittel, Thomas [1 ]
Meiners, Paul [2 ]
Geist, Andreas [1 ]
Panak, Petra J. [1 ,2 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Nucl Waste Disposal INE, POB 3640, D-76021 Karlsruhe, Germany
[2] Heidelberg Univ, Inst Phys Chem, Neuenheimer Feld 253, D-69120 Heidelberg, Germany
关键词
LIGANDS; CM(III); TRLFS; 2,6-BIS(5-(2,2-DIMETHYLPROPYL)-1H-PYRAZOL-3-YL)PYRIDINE; REAGENTS; ACTINIDE; EU(III); NUMBER; EU;
D O I
10.1039/d4ra05630b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To improve the understanding of the extraction chemistry of An(iii) and Ln(iii) with N-donor ligands 2,6-bis(5-(tert-butyl)-1H-pyrazol-3-yl)pyridine (C4-BPP) in the presence of 2-bromohexanoic acid was investigated. Extraction studies showed an excellent separation factor of SFAm(III)/Eu(III) approximate to 200 and SFAm(III)/Nd(III) approximate to 60 in comparison with the structurally similar ligand 2,6-bis(5-neopentyl-1H-pyrazol-3-yl)pyridine C5-BPP (SFAm(III)/Eu(III) approximate to 100), even though C5-BPP showed significantly higher stability constants. Time-resolved laser fluorescence spectroscopy (TRLFS) studies revealed the formation of the ternary 1 : 1 and 1 : 2 complexes [Eu(C4-BPP)(n)(2-bromohexanoate)(m)]((3-m)+) (n = 1-2) ( and ). [Eu(C4-BPP)(2)(2-bromohexanoate)(m)]((3-m)+) was the relevant complex species in solvent extraction. In contrast, Cm(iii) form stable 1 : 3 complexes. The ability of 2-bromohexanoic acid to replace C4-BPP from the inner coordination sphere of Eu(iii) but not from Cm(iii) is due to a more favorable complexation of Cm(iii) over Eu(iii) with C4-BPP. This resulted in a notably more efficient separation of An(iii) and Ln(iii) in comparison with C5-BPP.
引用
收藏
页码:28415 / 28422
页数:8
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