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 |
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Pages (from-to) | 3099-3102 |
Number of pages | 4 |
Journal | Organometallics |
Volume | 34 |
Issue number | 13 |
DOIs | |
State | Published - 13 Jul 2015 |