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Updated: Jun 14, 2025

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Extraction and complexation studies with 2,6-bis(5-(tert-butyl)-1H-pyrazol-3-yl)pyridine in the presence of
Jonas Stracke1,2, Patrik Weßling2, Thomas Sittel1
1Karlsruhe Institute of Technology (KIT), Institute for Nuclear Waste Disposal (INE) P.O. Box 3640 76021 Karlsruhe Germany Jonas.stracke@kit.edu.
Abstract:
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) ≈ 200 and SFAm(III)/Nd(III) ≈ 60 in comparison with the structurally similar ligand 2,6-bis(5-neopentyl-1H-pyrazol-3-yl)pyridine C5-BPP (SFAm(III)/Eu(III) ≈ 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) (2-bromohexanoate) ](3- (n = 1-2) ( and ). [Eu(C4-BPP)2(2-bromohexanoate) ](3- 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.
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