Aerobic intramolecular carbon-hydrogen bond oxidation promoted by Cu(I) complexes
María Álvarez1, Francisco Molina1, Manuel R Fructos1
1Laboratorio de Catálisis Homogénea, Unidad Asociada al CSIC CIQSO-Centro de Investigación en Química Sostenible and Departamento de Química, Universidad de Huelva, 21007-Huelva, Spain.
Abstract:
The oxidation of C-H bonds by copper centres in enzymes with molecular oxygen takes place in nature under ambient conditions. Herein we report a similar transformation in which under ambient pressure and temperature (1 atm, 25 °C) the complex TpMsCu(THF) (TpMs = hydrotris(3-mesityl-pyrazol-1-yl)borate) undergoes the intramolecular oxidation of an alkylic C-H bond with O2, leading to the formation of a trinuclear compound where alkoxy and hydroxyl ligands are bonded to the copper centres, as inferred from X-ray studies. The presence of adventitious Cu(0) derived from the partial decomposition of initial TpMsCu(THF) facilitates the formation of such a trinuclear compound. DFT studies support the reaction taking place through a Cu(iii) alkoxy-hydroxyl copper intermediate.
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