Selective Am(III)/Eu(III) Separation by Asymmetric Phenanthroline Derivatives with Lateral Phosphonate and Pyrazole Groups

The separation of trivalent americium from lanthanides poses a significant challenge for nuclear waste management. In this study, we present a series of novel asymmetric tetradentate ligands PO-PzPhen, i.e., diethyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L1 ), dibutyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L2 ), bis(2-ethylhexyl) (9-(1 H -pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L3 ), diphenyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L4 ), and diethyl (9-(4-methyl-1 H -pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L5 ), which integrate lateral phosphonate and pyrazolyl groups on a phenanthroline core. By introducing hard/soft donor synergy, L1 – L5 demonstrated robust extraction capabilities, high selectivity for Am(III) (SF Am/Eu reaching 49 for L3 ), and rapid extraction (equilibrium achieved within 10 min) under conditions of high acidity and favorable solubility in common diluents as well. The compositions of the extracted complexes, i.e., [ML(NO 3 ) 3 ] (M = Am(III) or Eu(III); L = L1 – L5 ), were characterized using slope analysis, high-resolution mass spectrometry, and time-resolved fluorescence spectroscopy. X-ray crystallographic analysis established the precise 1:1 (M:L) coordination geometry, demonstrating that all N- and O-donors are involved in the metal–ligand interaction. On the basis of these structural insights, DFT calculations were employed to further elucidate the mechanisms for the Am(III) selectivity and relatively rapid extraction kinetics, highlighting the lower rotation energy and enhanced intrinsic binding affinity toward actinides. This study demonstrates that the asymmetric ligands with multiple functional groups can synergistically optimize solvent extraction performance, providing an efficient framework for the advanced partitioning of trivalent minor actinides from high-level radioactive wastes.

Authors

Institutions

Publication Details

Journal
Inorganic Chemistry
Published
2026-06-25
DOI
https://doi.org/10.1021/acs.inorgchem.6c01181
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Selective Am(III)/Eu(III) Separation by Asymmetric Phenanthroline Derivatives with Lateral Phosphonate and Pyrazole Groups

Zongyuan Chen, Zhijun Guo, Qing Chang, Suliang Yang et al.
Inorganic Chemistry
Radioactive element chemistry and processing
article

Selective Am(III)/Eu(III) Separation by Asymmetric Phenanthroline Derivatives with Lateral Phosphonate and Pyrazole Groups

Zongyuan Chen, Zhijun Guo, Qing Chang, Suliang Yang, T Liu, J H Li, Hui Li, Zi Wang, Qiang Jin, Qiaorui Sui, Tengfei Cui, Zhen Xu, Chao Tang
article en

Abstract

The separation of trivalent americium from lanthanides poses a significant challenge for nuclear waste management. In this study, we present a series of novel asymmetric tetradentate ligands PO-PzPhen, i.e., diethyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L1 ), dibutyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L2 ), bis(2-ethylhexyl) (9-(1 H -pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L3 ), diphenyl (9-(1H-pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L4 ), and diethyl (9-(4-methyl-1 H -pyrazol-1-yl)-1,10-phenanthrolin-2-yl)phosphonate ( L5 ), which integrate lateral phosphonate and pyrazolyl groups on a phenanthroline core. By introducing hard/soft donor synergy, L1 – L5 demonstrated robust extraction capabilities, high selectivity for Am(III) (SF Am/Eu reaching 49 for L3 ), and rapid extraction (equilibrium achieved within 10 min) under conditions of high acidity and favorable solubility in common diluents as well. The compositions of the extracted complexes, i.e., [ML(NO 3 ) 3 ] (M = Am(III) or Eu(III); L = L1 – L5 ), were characterized using slope analysis, high-resolution mass spectrometry, and time-resolved fluorescence spectroscopy. X-ray crystallographic analysis established the precise 1:1 (M:L) coordination geometry, demonstrating that all N- and O-donors are involved in the metal–ligand interaction. On the basis of these structural insights, DFT calculations were employed to further elucidate the mechanisms for the Am(III) selectivity and relatively rapid extraction kinetics, highlighting the lower rotation energy and enhanced intrinsic binding affinity toward actinides. This study demonstrates that the asymmetric ligands with multiple functional groups can synergistically optimize solvent extraction performance, providing an efficient framework for the advanced partitioning of trivalent minor actinides from high-level radioactive wastes.

Inorganic Chemistry
China Institute of Atomic Energy (CN), International Isotopes (United States) (US), Lanzhou University (CN), Tsinghua University (CN)
National Natural Science Foundation of China, China National Nuclear Corporation, Fundamental Research Funds for the Central Universities
Clean water and sanitation
Openalex Percentile: Top 15%
Radioactive element chemistry and processing
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.