4.6 Article

Aerobic oxidation of glucose and 1-phenylethanol over gold nanoparticles directly deposited on ion-exchange resins

Journal

APPLIED CATALYSIS A-GENERAL
Volume 353, Issue 2, Pages 243-248

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2008.10.049

Keywords

Gold nanoparticles; Gold catalyst; Ion-exchange resin; Glucose oxidation; Alcohol oxidation

Funding

  1. Japan Science and Technology Agency (JST)
  2. Core Research for Evolutional Science and Technology (CREST)
  3. Gold Research Opportunities Worldwide (GROW) Programme of the World Gold Council
  4. Japan Society for the Promotion of Science [19850018]
  5. Grants-in-Aid for Scientific Research [19850018] Funding Source: KAKEN

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Gold nanoparticles (Au NPs) were deposited directly onto ion-exchange resins by reducing HAuCl4 or. Au(en)(2)Cl-3 (en = ethylenediamine) with NaBH4 or with surface amine and ammonium groups in anion-exchange resins. Catalytic activity for the oxidation of glucose and of 1-phenylethanol with molecular oxygen was more greatly influenced by the nature of polymer supports than by the size of Au NPs and increased in the order of the basicity of ion-exchange resins. Strongly basic anion-exchange resins such as quaternary ammonium salt (-N+Me3) functionalized resin exhibited a TOF (the reaction rate per loaded Au) as high as 27,000 h(-1) (7.5 s(-1)) for glucose oxidation at 60 degrees C and at pH 9.5. For 1-phenylethanol under base-free conditions, a TOF of 60 h(-1) was obtained at 60 degrees C, indicating that anion-exchange resins worked as solid bases. (C) 2008 Elsevier B.V. All rights reserved.

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