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Abstract / Description of output
New bonds for the uranyl: The controlled conversion of an uranyl oxo group ([UO2]+) into covalently bonded UOH and UOSi groups is described for pentavalent uranyl Pacman complexes. The unusual oxo–hydroxy motif is achieved by a protonation reaction and retains the normally unstable UV uranyl oxidation state. This product is readily silylated by treatment with a chlorosilane resulting in UOSi bond formation (see scheme).
Original language | English |
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Pages (from-to) | 9456-9458 |
Number of pages | 3 |
Journal | Angewandte Chemie International Edition |
Volume | 50 |
Issue number | 40 |
DOIs | |
Publication status | Published - Sept 2011 |
Keywords / Materials (for Non-textual outputs)
- actinides
- oxo functionalization
- pentavalent uranyl
- schiff-base macrocycle
- uranyl hydroxide
- LEWIS-ACID COORDINATION
- INFRARED-SPECTROSCOPY
- OXYGEN-EXCHANGE
- REDUCTION
- FUNCTIONALIZATION
- ACTIVATION
- HYDROXIDE
- CATALYSIS
- DICATION
- LIGAND
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Dive into the research topics of 'Oxo Group Protonation and Silylation of Pentavalent Uranyl Pacman Complexes'. Together they form a unique fingerprint.Projects
- 1 Finished
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Probing the chemistry of actinide cation-cation complexes
Arnold, P. & Love, J.
1/03/09 → 31/10/13
Project: Research