Influence of Electronic Modulation of Phenanthroline-Derived Ligands on Separation of Lanthanides and Actinides |
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Authors: | Ming-Ming Li Xiao-Juan Liu Qi Yang Yue-Kun Liu Jiang Nie Shu-Ming Yang Ya-Ya Yang Fu-Yan Lou Song-Tao Xiao Ying-Gen Ouyang Guo-An Ye |
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Affiliation: | Department of Radiochemistry, China Institute of Atomic Energy, P.O. Box 275, Beijing 102413, China; (M.-M.L.); (X.-J.L.); (Q.Y.); (Y.-K.L.); (J.N.); (S.-M.Y.); (Y.-Y.Y.); (F.-Y.L.); (S.-T.X.); (Y.-G.O.) |
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Abstract: | The solvent extraction, complexing ability, and basicity of tetradentate N-donor 2,9-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-1,2,4-benzotriazin-3-yl)-1,10-phenanthroline (CyMe4-BT- Phen) and its derivatives functionalized by Br, hydroxyphenyl, nitryl were discussed and compared. It was demonstrated that four BTPhen ligands are able to selectively extract Am(lll) over Eu(lll). It was notable that the distribution ratio of 5-nitryl-CyMe4-BTPhen for Eu(lll) was suppressed under 0.02, which was much lower compared to DEu(lll) = 1 by CyMe4-BTPhen. The analysis of the effect of the substituent on the affinity to lanthanides was conducted by UV/vis and fluorescence spectroscopic titration. The stability constants of various ligands with Eu(lll) were obtained by fitting titration curve. Additionally, the basicity of various ligands was determined to be 3.1 ± 0.1, 2.3 ± 0.2, 0.9 ± 0.2, 0.5 ± 0.1 by NMR in the media of CD3OD with the addition of DClO4. The basicity of ligands follows the order of L1 > L2 > L3 > L4, indicating the tendency of protonation decreases with the electron-withdrawing ability increase. |
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Keywords: | separation solvent extraction lanthanides ligand phenanthroline |
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