Theoretical Study on the Coordination and Separation Capacity of Macrocyclic N-Donor Extractants for Am(III)/Eu(III).

Designing ligands that can effectively separate actinide An(III)/lanthanide Ln(III) in the solvent extraction process remains one of the key issues in the treatment of accumulated spent nuclear fuel. Nitrogen donor ligands are considered as promising extractants for the separation of An(III) and Ln(III) due to their environmental friendliness. Four new macrocyclic N-donor hexadentate extractants were designed and their coordination with Am(III) and Eu(III), as well as their extraction selectivity and separation performance for Am(III) and Eu(III), were investigated by scalar relativistic density functional theory. A variety of theoretical methods have been used to evaluate the properties of the four ligands and the coordination structures, bonding properties, and thermodynamic properties of the complexes formed by the four ligands with Am(III) and Eu(III). The results of various wavefunction analysis methods including NBO analysis, quantum theory of atoms in molecules (QTAIM) analysis, and so on show that Am(III) has a stronger coordination ability with the ligands than Eu(III) due to the Am 5f orbitals more involved in bonding with the ligands than the Eu 4f orbitals, and the bonding environment of the N-donor in the ligand has a significant effect on its coordination ability of the metal ions. Thermodynamic analysis of the solvent extraction process shows that all of the four N-containing macrocyclic ligands have good extraction selectivity and separation performance for Am(III) and Eu(III). This study provides theoretical support for designing potential nitrogen-containing macrocyclic extractants with excellent separation performance.

Oxidative Dehydrogenation of Hydrazobenzenes toward Azo Compounds Catalyzed by tert-Butyl Nitrite in EtOH.

We describe a tert-butyl nitrite-catalyzed oxidative dehydrogenation of hydrazobenzenes for producing azobenzenes. This method proceeds at ambient temperature and under an atmospheric environment by employing eco-friendly EtOH as the medium, representing a mild, general route to the synthesis of various symmetrical and nonsymmetrical azobenzenes in excellent yields with broad functional group tolerance.