Coordination of Fluorine-Substituted 1,10-Phenanthroline Diphosphonates with Americium(III) and Lanthanides(III): Solvent Extraction, Complexation, XRD, and Theoretical Study

Hybrid N,O-donor ligands based on 1,10-phenanthroline are a promising class of compounds for processing high-level waste. Here, we synthesized novel phenanthroline-based diphosphonates containing electron-withdrawing fluorine atoms in alkyl substituents. We studied their extraction properties for Am(III) and, for the first time, for the entire series of lanthanides(III). The extraction of nitric acid for these diphosphonates was also studied. It has been shown that replacing one hydrogen atom with a fluorine atom in the ethyl substituent of a diphosphonate leads to a decrease in the affinity of the ligands for metal cations. Replacing two hydrogen atoms leads to a decrease in the affinity of the ligands for both metal cations and protons. But such modifications led to a change in the nature of the extraction of Am(III) and Eu(III) from nitric acid solutions, and as a result, the diphosphonate with two substituted hydrogen atoms retains its extraction properties when extracted from 5 mol/L HNO