Hu Shu-Xian, Li Wan-Lu, Dong Liang, Gibson John K, Li Jun
Beijing Computational Science Research Center, Beijing 100193, China.
Department of Chemistry and Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education, Tsinghua University, Beijing 100084, China.
Dalton Trans. 2017 Sep 28;46(36):12354-12363. doi: 10.1039/c7dt02825c. Epub 2017 Sep 11.
For further fundamental understanding of the nature and extent of covalency in actinyl-ligand bonding, and the benefits that this may have in the design of new ligands for nuclear waste separation, there is burgeoning interest in the nature of actinyl complexes with polydentate or multiple-point-donor ligands, such as crown ethers. There are few cases of structurally authenticated molecular actinyl-crown bonds under ambient conditions. We report here the computational characterization of AnO-(15-crown-5) complexes, where An = U, Np, Pu, Am, and Cm, and 15-crown-5 is the cyclic polyether ligand with five ether oxygen atoms. In the gas-phase complex, the actinyl group is located inside of the crown ether, tilted slightly out of the plane of the five equatorial oxygen atoms that coordinate the actinide metal center. The actinyl-cyclic ether complexes are found to exhibit a conventional conformation, with typical An-O and An-O distances and angles. A striking result is the enhanced stability of the insertion complex for UOversus NpO, PuO, AmO and CmO, which is evaluated in the context of An-O binding strengths (esp. bonding covalency), and may have ramifications for the utility of actinyl-crown complexes in separation applications.
为了进一步从根本上理解锕酰-配体键合中共价性的本质和程度,以及这在设计用于核废料分离的新配体时可能带来的益处,人们对锕酰与多齿或多点供体配体(如冠醚)形成的配合物的本质产生了浓厚兴趣。在环境条件下,经过结构验证的分子锕酰-冠醚键的情况很少。我们在此报告AnO-(15-冠-5)配合物的计算表征,其中An = U、Np、Pu、Am和Cm,15-冠-5是具有五个醚氧原子的环状聚醚配体。在气相配合物中,锕酰基团位于冠醚内部,略微倾斜于与锕系金属中心配位的五个赤道氧原子所在的平面。发现锕酰-环醚配合物呈现出传统构象,具有典型的An-O键长和键角。一个显著的结果是,相对于NpO、PuO、AmO和CmO,UO的插入配合物稳定性增强,这是在An-O结合强度(特别是键合共价性)的背景下评估的,并且可能对锕酰-冠醚配合物在分离应用中的效用产生影响。