Abstract
Oxygenation of 1,5-cyclooctadiene (COD) is achieved on an iridium center using water as a reagent. A hydrogen-bonding interaction with an unbound nitrogen atom of the naphthyridine-based ligand architecture promotes nucleophilic attack of water to the metal-bound COD. Irida-oxetane and oxo-irida-allyl compounds are isolated, products which are normally accessed from reactions with H 2 O 2 or O 2. DFT studies support a ligand-assisted water activation mechanism.
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CITATION STYLE
Ghatak, T., Sarkar, M., Dinda, S., Dutta, I., Rahaman, S. M. W., & Bera, J. K. (2015). Olefin oxygenation by water on an iridium center. Journal of the American Chemical Society, 137(19), 6168–6171. https://doi.org/10.1021/jacs.5b03055
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