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Abstract
The synthesis of a series of digold hydroxide complexes is reported. These diaurated species, of the formula [{Au(NHC)}2(μ-OH)][BF4] (where NHC = IPrCl, IPr*, IPent), were easily prepared via the cationic species [Au(NHC)(NCCH3)][BF4] in aqueous media. The catalytic activity of these novel complexes was tested and compared to that of the previously reported IPr and SIPr derivatives. These digold hydroxide species are highly active in water-inclusive organic transformations, such as the alkyne and nitrile hydration reactions, and the Meyer–Schuster rearrangement. One salient feature of these systems is the lack of any additive to induce catalytic activity.
Original language | English |
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Pages (from-to) | 1106-1111 |
Number of pages | 6 |
Journal | Organometallics |
Volume | 32 |
Issue number | 4 |
Early online date | 6 Feb 2013 |
DOIs | |
Publication status | Published - 25 Feb 2013 |
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Dive into the research topics of '[{Au(NHC)}2(μ-OH)][BF4]: Silver-Free and Acid-Free Catalysts for Water-Inclusive Gold-Mediated Organic Transformations'. Together they form a unique fingerprint.Projects
- 1 Finished
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EPSRC - EP/J011053/1- LATE TRANSITION: Late Transition Metal Hydroxide in Homogeneous Catalysis
Nolan, S. P. (PI)
15/03/12 → 14/03/15
Project: Standard