Abstract
A DFT study of the reduction and silylation of the uranyl U-O bond in a macrocyclic complex shows the importance of the initial dipotassiation in THF solution, and a slightly downhill reaction pathway for the oxo group functionalisation.
Original language | English |
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Pages (from-to) | 2402-2404 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 17 |
DOIs | |
Publication status | Published - 2009 |
Keywords / Materials (for Non-textual outputs)
- PENTAVALENT-URANYL
- ACTINYL IONS
- CHEMISTRY
- URANIUM
- COORDINATION
- COMPLEXES
- MECHANISM
- CP2UO
- OXIDE
- TH