A series of 1,2-N-substituted o-carboranes were obtained. Ultra-long C–C distances were found in the secondary-amino o-carboranes 3. The relationship between C–C bond lengths and the electron effects of the benzyl groups was discussed.
Main observation and conclusion
The steric and electronic properties of N‐heterocyclic carbenes (NHCs) can be modified by the exocyclic substituents at the nitrogen atoms, by 1—3 atoms’ replacements of the five‐membered imidazolium skeleton and by the changes of the backbones. Herein, we report the usage of nido‐C2B9 carborane anions as the backbones of NHCs. Stirring the mixture of secondary amino o‐carboranes (1b—1e), triethyl orthoformate and HBF4∙Et2O results in the unexpected cage‐opening of o‐carboranes to afford the nido‐C2B9 carborane anions supported N‐heterocyclic carbene precursors (4b—4e). Deprotonation of 4b with sodium hexamethyldisilazide at −78 oC affords the N‐heterocyclic carbene ligand, which was used to form an Au(I) NHC complex (5). DFT calculations revealed a high‐lying lone pair orbitals of the carbene ligands, predicting their strong σ‐donating abilities.
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