Abstract
A rare three-coordinate germanone [IPrN]2Ge=O (IPrN=bis(2,6-diisopropylphenyl)imidazolin-2-imino) was successfully isolated. The germanone has a rather high thermal stability in arene solvent, and no detectable change was observed at 80 °C for at least one week. However, high thermal stability of [IPrN]2Ge=O does not prevent its reactivity toward small molecules. Structural analysis and initial reactivity studies revealed the highly polarized nature of the terminal Ge=O bond. Besides, the addition of phenylacetylene, as well as O-atom transfer with 2,6-dimethylphenyl isocyanide make it a mimic of nucleophilic transition-metal oxides. Mechanism for O-atom transfer reaction was investigated via DFT calculations, which revealed that the reaction proceeds via a [2+2] cycloaddition intermediate.
Original language | English |
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Pages (from-to) | 15914-15917 |
Number of pages | 4 |
Journal | Chemistry - A European Journal |
Volume | 27 |
Issue number | 64 |
DOIs | |
State | Published - 17 Nov 2021 |
Keywords
- N-heterocyclic imines
- O-atom transfer
- carbonyls
- germanone
- small molecule activation