Abstract
Despite steady progress in catalytic methods for the borylation of hydrocarbons, methane has not yet been subject to this transformation. Here we report the iridium-catalyzed borylation of methane using bis(pinacolborane) in cyclohexane solvent. Initially, trace amounts of borylated products were detected with phenanthroline-coordinated Ir complexes. A combination of experimental high-pressure and high-throughput screening, and computational mechanism discovery techniques helped to rationalize the foundation of the catalysis and identify improved phosphine-coordinated catalytic complexes. Optimized conditions of 150°C and 3500-kilopascal pressure led to yields as high as ∼52%, turnover numbers of 100, and improved chemoselectivity for monoborylated versus diborylated methane.
Cite
CITATION STYLE
Smith, K. T., Berritt, S., González-Moreiras, M., Ahn, S., Smith, M. R., Baik, M. H., & Mindiola, D. J. (2016). Catalytic borylation of methane. Science, 351(6280), 1424–1427. https://doi.org/10.1126/science.aad9730
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.