Lewis Andrew J, Yin Haolin, Carroll Patrick J, Schelter Eric J
Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, PA, USA.
Dalton Trans. 2014 Jul 28;43(28):10844-51. doi: 10.1039/c4dt00763h.
Directed coordination of weakly Lewis acidic K(+) ions to weakly Lewis basic uranyl oxo ligands is accomplished through non-covalent cation-π and cation-F interactions for the first time. Comparison of a family of structurally related diarylamide ligands highlights the role that the cation-π and cation-F interactions play in guiding coordination. Cation binding to uranyl is demonstrated in the solid state and in solution, providing the shortest reported crystallographic uranyl-oxo to potassium distance. UV-Vis, TD-DFT calculations, and electrochemical measurements show that cation coordination directly impacts the electronics at the uranium(vi) cation.
首次通过非共价阳离子-π和阳离子-氟相互作用实现了弱路易斯酸性钾离子与弱路易斯碱性铀酰氧配体的定向配位。一系列结构相关的二芳基酰胺配体的比较突出了阳离子-π和阳离子-氟相互作用在引导配位中所起的作用。在固态和溶液中均证明了阳离子与铀酰的结合,提供了报道的最短晶体学铀酰氧至钾的距离。紫外可见光谱、含时密度泛函理论计算和电化学测量表明,阳离子配位直接影响铀(VI)阳离子处的电子性质。