化学
铕
滴定法
密度泛函理论
萃取(化学)
镅
溶剂
锕系元素
苯
结晶学
配体(生物化学)
物理化学
无机化学
计算化学
有机化学
离子
受体
生物化学
作者
Jieru Wang,Dongping Su,Dongqi Wang,Songdong Ding,Chao Huang,Huang Huang,Xiao-Yang Hu,Zhipeng Wang,Shimeng Li
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2015-10-30
卷期号:54 (22): 10648-10655
被引量:31
标识
DOI:10.1021/acs.inorgchem.5b01452
摘要
1,3-Bis[3-(2-pyridyl)pyrazol-1-yl]propane (Bippp) and 1,2-bis[3-(2-pyridyl)pyrazyl-1-methyl]benzene (Dbnpp), the pyridylpyrazole based tetradentate ligands, were synthesized and characterized by MS, NMR, and FT-IR. The solvent extraction and complexation behaviors of Am(III) and Eu(III) with the ligands were investigated experimentally and theoretically. In the presence of 2-bromohexanoic acid, the two ligands can effectively extract Am(III) over Eu(III) and other rare earth(III) metals (RE(III)) in HNO3 solution with the separation factors (SFAm/RE) ranging from 15 to 60. Slope analyses showed that both Am(III) and Eu(III) were extracted as monosolvated species, which agrees well with the results observed from X-ray crystallography and MS analyses. The stability constants (log K) obtained from UV–vis titration for Eu(III) complexes with Bippp and Dbnpp are 4.75 ± 0.03 and 4.45 ± 0.04, respectively. Both UV–vis titration and solvent extraction studies indicated that Bippp had stronger affinity for Eu(III) than Dbnpp, which is confirmed by density functional theory (DFT) calculations. DFT calculations revealed that the AmL(NO3)3 (L = Bippp and Dbnpp) complexes are thermodynamically more stable in water than their Eu(III) analogues, which is caused by greater covalency of the Am–N than Eu–N bonds. Theoretical studies gave an insight into the nature of the M(III)–ligand bonding interactions.
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