Abstract
The reaction between non-aqueous uranyl silylamide (UO2[N(SiMe3)2]2·2THF) under anaerobic conditions or uranyl acetate (UO2(OAc)2·2H2O) under standard laboratory conditions and dipyriamethryin affords a bench-stable uranyl complex. Competition studies as well as DFT calculations provide support for the observed selectivity for the uranyl cation over trivalent lanthanide and multiple transition metal precursors.
Original language | English |
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Pages (from-to) | 4981-4984 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 53 |
Issue number | 36 |
DOIs | |
Publication status | Published - 2017 |
Externally published | Yes |