Autor: |
Cui Tengfei, Haolong Wang, Zhijun Guo, Wang Yin, Jixue Sui, Pavle Mocilac |
Rok vydání: |
2022 |
Předmět: |
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Zdroj: |
Separation and Purification Technology. 282:120046 |
ISSN: |
1383-5866 |
DOI: |
10.1016/j.seppur.2021.120046 |
Popis: |
Four asymmetric alkyl-substituted DAPhens (N,N’-Dimethyl-N,N’-Dialkyl-2,9-Diamide-1,10-Phenanthrolines) were synthesized and investigated as selective ligands for UO22+. The results confirm that the ligands have higher affinity for uranyl comparing to the symmetric analogues with the same 1,10-phenanthroline core moiety. The slope analysis indicated the formation of 1:1 (metal/ligand) extracting complex, which was identified in the organic phase as [UO2(DAPhen-4)(NO3)]+ complex ion by electrospray ionization mass spectrometry (ESI-MS). The superior affinity of the ligands for UO22+ over Th4+ and Eu3+ in solvent extraction was consistent with the stability constants of their complexes in acetonitrile obtained by UV–Vis spectroscopic titrations. The observed better affinity of the asymmetric alkyl-substituted DAPhens could originate from the less steric hindrance of methyl in the terminal groups, which was confirmed by the relatively mild distortion of the ligand structure in the uranyl complex according to the crystal and molecular structure of the solid-state complex [UO2(DAPhen-1)(NO3)](NO3)·(CH3OH) as characterized by single crystal X-ray diffraction. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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