Department of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, UK.
J Am Chem Soc. 2011 Aug 24;133(33):13093-102. doi: 10.1021/ja203378m. Epub 2011 Aug 2.
The synthesis, lanthanide complexation, and solvent extraction of actinide(III) and lanthanide(III) radiotracers from nitric acid solutions by a phenanthroline-derived quadridentate bis-triazine ligand are described. The ligand separates Am(III) and Cm(III) from the lanthanides with remarkably high efficiency, high selectivity, and fast extraction kinetics compared to its 2,2'-bipyridine counterpart. Structures of the 1:2 bis-complexes of the ligand with Eu(III) and Yb(III) were elucidated by X-ray crystallography and force field calculations, respectively. The Eu(III) bis-complex is the first 1:2 bis-complex of a quadridentate bis-triazine ligand to be characterized by crystallography. The faster rates of extraction were verified by kinetics measurements using the rotating membrane cell technique in several diluents. The improved kinetics of metal ion extraction are related to the higher surface activity of the ligand at the phase interface. The improvement in the ligand's properties on replacing the bipyridine unit with a phenanthroline unit far exceeds what was anticipated based on ligand design alone.
本文描述了一种菲咯啉衍生的四齿双三嗪配体,用于从硝酸溶液中合成、镧系元素配位和溶剂萃取锕系元素(III)和镧系元素(III)放射性示踪剂。与 2,2'-联吡啶配体相比,该配体具有非常高的分离效率、高选择性和快速萃取动力学,能够将 Am(III) 和 Cm(III) 与镧系元素分离。通过 X 射线晶体学和力场计算分别阐明了配体与 Eu(III) 和 Yb(III) 的 1:2 双配合物的结构。Eu(III)双配合物是第一个通过晶体学表征的四齿双三嗪配体的 1:2 双配合物。通过在几种稀释剂中使用旋转膜池技术进行动力学测量,验证了更快的萃取速率。金属离子萃取动力学的改善与配体在相界面处更高的表面活性有关。用菲咯啉单元取代联吡啶单元,配体性能的提高远远超过仅基于配体设计的预期。