Abstract
A comparison of Rh and Ir complexes of the SiNN ligand (combining Si-H, amido, and quinoline donors) reveals its great degree of adaptability. The amido donor can function as a boryl group acceptor, and the Si-H/metal interaction is highly variable. In contrast to Ir analogues, complexes of Rh do not catalyze dehydrogenative borylation of terminal alkynes but do act as modest benzene borylation catalysts.
| Original language | English |
|---|---|
| Pages (from-to) | 3099-3102 |
| Number of pages | 4 |
| Journal | Organometallics |
| Volume | 34 |
| Issue number | 13 |
| DOIs | |
| State | Published - 13 Jul 2015 |