Schöne Sebastian, Radoske Thomas, März Juliane, Stumpf Thorsten, Patzschke Michael, Ikeda-Ohno Atsushi
Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Institute of Resource Ecology, Bautzner Landstraße 400, 01328, Dresden, Germany.
Chemistry. 2017 Oct 4;23(55):13574-13578. doi: 10.1002/chem.201703009. Epub 2017 Sep 5.
A simple synthesis based on UO Cl ⋅n H O and 1,10-phenanthroline (phen) resulted in the formation of a new uranyl(VI) complex [UO Cl (phen) ] (1), revealing a unique dodecadeltahedron coordination geometry around the uranium center with significant bending of the robust linear arrangement of the uranyl (O-U-O) unit. Quantum chemical calculations on complex 1 indicated that the weak but distinct interactions between the uranyl oxygens and the adjacent hydrogens of phen molecules play an important role in forming the dodecadeltahedron geometry that fits to the crystal structure of 1, resulting in the bending the uranyl unit. The uranyl oxygens in 1 are anticipated to be activated as compared with those in other linear uranyl(VI) compounds.
基于UOCl·nH₂O和1,10-菲咯啉(phen)的简单合成方法得到了一种新的铀酰(VI)配合物[UOCl₂(phen)₂](1),该配合物在铀中心周围呈现出独特的十二面体配位几何结构,铀酰(O-U-O)单元的稳健线性排列发生了显著弯曲。对配合物1的量子化学计算表明,铀酰氧原子与邻菲咯啉分子相邻氢原子之间微弱但明显的相互作用在形成与配合物1晶体结构相匹配的十二面体几何结构中起着重要作用,导致铀酰单元发生弯曲。与其他线性铀酰(VI)化合物相比,预计配合物1中的铀酰氧原子具有更高的活性。