Tharp Eralie Dylan M, Hiti Ethan A, Bhakta Dev T, Williamson Justin A, Gorden John D, Vasylevskyi Serhii, Gorden Anne E V
Texas Tech University, Department of Chemistry and Biochemistry, Lubbock, Texas, United States, 79401.
Inorg Chem. 2025 Jan 13;64(1):731-740. doi: 10.1021/acs.inorgchem.4c02843. Epub 2024 Dec 19.
Uranium is most stable when it is exposed to oxygen or water in its +6 oxidation state as the uranyl (UO) ion. This ion is subsequently particularly stable and very resistant to functionalization due to the inverse trans effect. Uranyl oxo ligands are typically not considered good hydrogen bond acceptors due to their weak Lewis basicity; however, the ligands bound in the equatorial plane greatly affect the strength of the oxo ligands' hydrogen bonding. In this work, new naphthylsalophen and pyrasal complexes of uranium were synthesized and crystallized for characterization in the solid state. The bond lengths and angles of the uranyl ion and the ligand conformation are compared. In the solid state, one of the pyrasal complexes showed a hydrogen bond directly from a water molecule to the uranyl oxo ligand, which resulted in an asymmetric lengthening of the U-O bonds from 1.789 to 1.862 Å and 1.784 to 1.844 Å.
铀在以铀酰(UO)离子的+6氧化态暴露于氧气或水时最为稳定。由于反位效应,该离子随后特别稳定且对功能化具有很强的抗性。铀酰氧配体通常因其弱路易斯碱性而不被视为良好的氢键受体;然而,赤道平面上结合的配体极大地影响了氧配体氢键的强度。在这项工作中,合成了新的铀萘基水杨醛缩邻氨基酚和吡啶醛配合物,并使其结晶以进行固态表征。比较了铀酰离子的键长和键角以及配体构象。在固态中,一种吡啶醛配合物显示出一个水分子直接与铀酰氧配体形成氢键,这导致U - O键不对称地从1.789 Å延长至1.862 Å以及从1.784 Å延长至1.844 Å。