铀酰
共价键
化学
配位复合体
组合化学
结晶学
金属
有机化学
离子
作者
Andrew J. Lewis,Haolin Yin,Patrick J. Carroll,Eric J. Schelter
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2014-01-01
卷期号:43 (28): 10844-10851
被引量:20
摘要
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.
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