DFT Study of Americium and Europium Complexation with 2,9-Bis(1,2,4-triazin-3-yl)-1,10-Phenanthroline Ligand: The Influence of the Counteranions–Nitrate Versus Perchlorate
Jaanus Burk, Lauri Sikk, Kaido Tämm, Peeter Burk

TL;DR
This study explains why americium forms stronger complexes with a specific ligand than europium, using computational methods to match experimental results.
Contribution
The study reveals how counteranions and solvation affect the stability of americium and europium complexes with BTPhen ligand.
Findings
Europium forms more stable complexes with BTPhen ligand in the absence of anions and water.
Americium complexes with BTPhen become more stable when anions and water are present.
Nitrate counterions favor americium over europium complexation more than perchlorate.
Abstract
2,9-Bis(1,2,4-triazin-3-yl)-1,10-phenanthroline (BTPhen)-based ligands show great promise in the separation of trivalent lanthanides and actinides. Experimental studies have shown that americium forms stronger complexes with the BTPhen ligands than europium; most theoretical studies have so far failed to reproduce these results. In the current study, three different metal forms (the naked cation, its nitrate or perchlorate salts and tetraaqua solvated salts) were used to study different complexation reactions. It was shown that in the case of naked cations and salts, europium forms the most stable complex with the 2,9-bis(1,2-triazin-3-yl)-1,10-phenanthroline ligand in all of the reactions compared. However, europium is also more strongly interacting (compared to americium) with anions and water molecules in the tetraaquatrinitrato or tetraaquatriperchlorato complexes. That shifts the…
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Taxonomy
TopicsRadioactive element chemistry and processing · Lanthanide and Transition Metal Complexes · Chemical Synthesis and Characterization
