O'Connell-Danes Joseph, Ngwenya Bryne T, Morrison Carole A, Nichol Gary S, Delmau Lætitia H, Love Jason B
EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh EH9 3FJ, U.K.
School of Geosciences, University of Edinburgh, Edinburgh EH9 3FE, U.K.
JACS Au. 2024 Feb 12;4(2):798-806. doi: 10.1021/jacsau.3c00793. eCollection 2024 Feb 26.
Improving actinide separations is key to reducing barriers to medical and industrial actinide isotope production and to addressing the challenges associated with the reprocessing of spent nuclear fuel. Here, we report the first example of a supramolecular anion recognition process that can achieve this goal. We have designed a preorganized triamidoarene receptor that induces quantitative precipitation of the early actinides Th(IV), Np(IV), and Pu(IV) from industrially relevant conditions through the formation of self-assembled hydrogen-bonded capsules. Selectivity over the later An(III) elements is shown through modulation of the nitric acid concentration, and no precipitation of actinyl or transition-metal ions occurs. The Np, Pu, and Am precipitates were characterized structurally by single-crystal X-ray diffraction and reveal shape specificity of the internal hydrogen-bonding array for the encapsulated hexanitratometalates. This work complements ion-exchange resins for 5f-element separations and illustrates the significant potential of supramolecular separation methods that target anionic actinide species.
改进锕系元素的分离对于降低医学和工业用锕系元素同位素生产的障碍以及应对与乏核燃料后处理相关的挑战至关重要。在此,我们报道了一个能够实现这一目标的超分子阴离子识别过程的首个实例。我们设计了一种预组织的三酰胺芳烃受体,它通过形成自组装氢键胶囊,从工业相关条件下定量沉淀出早期锕系元素钍(IV)、镎(IV)和钚(IV)。通过调节硝酸浓度显示出对后期锕系(III)元素的选择性,并且没有发生锕酰离子或过渡金属离子的沉淀。通过单晶X射线衍射对镎、钚和镅沉淀物进行了结构表征,揭示了内部氢键阵列对包封的六硝酸根合金属酸盐的形状特异性。这项工作补充了用于5f元素分离的离子交换树脂,并说明了针对阴离子锕系元素物种的超分子分离方法的巨大潜力。