Oxy-functionalization of nucleophilic rhenium(I) metal carbon bonds catalyzed by selenium(IV)
William J., III Tenn, Brian L. Conley, Claas H. Hovelmann, Marten Ahlquist, Robert J. Nielsen, Daniel H. Ess, Jonas Oxgaard, Steven M. Bischof, William A. Goddard III, Roy A. Periana
Abstract
We report that SeO_2 catalyzes the facile oxy-functionalization of (CO)_5Re(I)-Me^(δ−) with IO_4− to generate methanol. Mechanistic studies and DFT calculations reveal that catalysis involves methyl group transfer from Re to the electrophilic Se center followed by oxidation and subsequent reductive functionalization of the resulting CH_3Se(VI) species. Furthermore, (CO)_3Re(I)(Bpy)-R (R = ethyl, n-propyl, and aryl) complexes show analogous transfer to SeO_2 to generate the primary alcohols. This represents a new strategy for the oxy-functionalization of M−R^(δ−) polarized bonds.
Group Members
Tenn, W. J. I., Conley, B. L., Hovelmann, C. H., Ahlquist, M., Nielsen, R. J., Ess, D. H., Oxgaard, J., Bischof, S. M., III, W. A. G., & Periana, R. A. (2009). Oxy-functionalization of nucleophilic rhenium(I) metal carbon bonds catalyzed by selenium(IV). *J. Am. Chem. Soc.*, *131*(7), 2466-2468. https://doi.org/10.1021/ja806814c