Catalytic borylation of methane

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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 degrees C and 3500-kilopascal pressure led to yields as high as similar to 52%, turnover numbers of 100, and improved chemoselectivity for monoborylated versus diborylated methane
Publisher
AMER ASSOC ADVANCEMENT SCIENCE
Issue Date
2016-03
Language
English
Article Type
Article
Keywords

C-H BONDS; ORGANOMETALLIC CHEMISTRY; ACETIC-ACID; ACTIVATION; COMPLEXES; FUNCTIONALIZATION; CONVERSION; CH4; HYDROCARBONS; FRONTIER

Citation

SCIENCE, v.351, no.6280, pp.1424 - 1427

ISSN
0036-8075
DOI
10.1126/science.aad9730
URI
http://hdl.handle.net/10203/208659
Appears in Collection
CH-Journal Papers(저널논문)
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