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The ability of Au catalysts to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cyclooctene is fascinating. Although supported nanometre-size Au particles are poorly active, here we show that solubilized atomic Au clusters, present in

The ability of Au catalysts to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cyclooctene is fascinating. Although supported nanometre-size Au particles are poorly active, here we show that solubilized atomic Au clusters, present in ng ml-1 concentrations and stabilized by ligands derived from the oxidized hydrocarbon products, are active. They can be formed from various Au sources. They generate initiators and propagators to trigger the onset of the auto-oxidation reaction with an apparent turnover frequency of 440 s-1, and continue to generate additional initiators throughout the auto-oxidation cycle without direct participation in the cycle. Spectroscopic characterization suggests that 7–8 atom clusters are effective catalytically. Extension of work based on these understandings leads to the demonstration that these Au clusters are also effective in selective oxidation of cyclohexene, and that solubilized Pt clusters are also capable of generating initiators for cyclooctene epoxidation.

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    Title
    • Stable and Solubilized Active Au Atom Clusters for Selective Epoxidation of Cis-Cyclooctene With Molecular Oxygen
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    Date Created
    2017-03-28
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    Identifier
    • Digital object identifier: 10.1038/ncomms14881
    • Identifier Type
      International standard serial number
      Identifier Value
      2041-1723
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    • The final version of this article, as published in Nature Communications, can be viewed online at: https://www.nature.com/articles/ncomms14881

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    Qian, L., Wang, Z., Beletskiy, E. V., Liu, J., Santos, H. J., Li, T., . . . Kung, H. H. (2017). Stable and solubilized active Au atom clusters for selective epoxidation of cis-cyclooctene with molecular oxygen. Nature Communications, 8, 14881. doi:10.1038/ncomms14881

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