Strong Periodic Tendency of Trivalent Lanthanides Coordinated with a Phenanthroline-Based Ligand: Cascade Countercurrent Extraction, Spectroscopy, and Crystallography

• Published in: Inorganic chemistry Vol. 60; no. 13; pp. 9745 - 9756
• Main Authors: Yang, Xiao-Fan, Ren, Peng, Yang, Qi, Geng, Jun-Shan, Zhang, Jin-Yu, Yuan, Li-Yong, Tang, Hong-Bin, Chai, Zhi-Fang, Shi, Wei-Qun
• Format: Journal Article
• Language: English
• Published: American Chemical Society 05.07.2021
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.1c01035

Phenanthroline-diamide ligands have been reported in the selective separation of actinides over Eu­(III); on the contrary, relevant basic coordination chemistry studies are still limited, and extraction under actual application conditions is rarely involved. In this work, N,N′-diethyl-N,N′-ditolyl-2,9-diamide-1,10-phenanthroline [Et-Tol-DAPhen (L)] was applied to explore the coordination performance of lanthanides in simulative high-level liquid waste. For the first time, cascade countercurrent extraction was conducted with Et-Tol-DAPhen as the extractant, which reveals the periodic tendency of the extraction efficiency of lanthanides to decrease gradually as the atomic number increases. Comparison of elements with similar radii verifies the hypothesis that the increase in the atomic number leads to a decrease in the ionic radius, thus reducing the coordination and extraction capacity of ligands. Slope analysis, electrospray ionization mass spectrometry, and ultraviolet–visible titration results show that the ligand forms 1:1 and 1:2 complexes with lanthanides and the coordination ability follows the tendency of extraction efficiency, and the first crystal structures of Lns­(III) with a phenanthroline-diamide ligand, i.e., [LaL(NO3)3(H2O)] and [LaL 2(NO3)2]­[(NO3)], were obtained, which confirms the conclusions described above. This work promises to enhance our comprehension of the chemical properties of Lns­(III) and offer new clues for the design and synthesis of novel separation ligands.