Abstract
A carborane-fused silylene 1-{[PhC(NtBu)2]Si}-1,2-C2B10H11 (2) has been prepared and structurally characterized from an equimolar reaction of 1-Li-1,2-C2B10H11 with [PhC(NtBu)2]SiCl (1) in Et2O. The reactions of 2 with elemental sulfur and benzophenone afforded the corresponding o-carborane substituted silanethione (3) and silaoxirane (4), respectively. On the other hand, the reaction of 2 with 2-benzoylpyridine led to the isolation of an unexpected compound 5 featuring a SiC2O2 five-membered ring. All new compounds were characterized by multiple NMR spectroscopic techniques and single-crystal X-ray analyses.
| Original language | English |
|---|---|
| Pages (from-to) | 173-177 |
| Number of pages | 5 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 865 |
| DOIs | |
| Publication status | Published - 15 Jun 2018 |
User-Defined Keywords
- Boron cluster
- Carborane
- Main group element
- Silicon
- Silylene