Resumen
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.
Idioma original | Inglés |
---|---|
Páginas (desde-hasta) | 4981-4984 |
Número de páginas | 4 |
Publicación | Chemical Communications |
Volumen | 53 |
N.º | 36 |
DOI | |
Estado | Publicada - 2017 |
Publicado de forma externa | Sí |