Gold-catalyzed oxidation of substituted phenols by hydrogen peroxide
KAUST DepartmentKAUST Catalysis Center (KCC)
Permanent link to this recordhttp://hdl.handle.net/10754/565982
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AbstractGold nanoparticles deposited on inorganic supports are efficient catalysts for the oxidation of various substituted phenols (2,6-di-tert-butyl phenol and 2,3,6-trimethyl phenol) with aqueous hydrogen peroxide. By contrast to more conventional catalysts such as Ti-containing mesoporous silicas, which convert phenols to the corresponding benzoquinones, gold nanoparticles are very selective to biaryl compounds (3,3′,5,5′-tetra-tert-butyl diphenoquinone and 2,2′,3,3′,5,5′-hexamethyl-4,4′- biphenol, respectively). Products yields and selectivities depend on the solvent used, the best results being obtained in methanol with yields >98%. Au offers the possibility to completely change the selectivity in the oxidation of substituted phenols and opens interesting perspectives in the clean synthesis of biaryl compounds for pharmaceutical applications. © 2010 Elsevier B.V. All rights reserved.
CitationCheneviere, Y., Caps, V., & Tuel, A. (2010). Gold-catalyzed oxidation of substituted phenols by hydrogen peroxide. Applied Catalysis A: General, 387(1-2), 129–134. doi:10.1016/j.apcata.2010.08.018
JournalApplied Catalysis A: General