4.8 Article

Tandem Dehydrogenation of Ammonia Borane and Hydrogenation of Nitro/Nitrile Compounds Catalyzed by Graphene-Supported NiPd Alloy Nanoparticles

Journal

ACS CATALYSIS
Volume 4, Issue 6, Pages 1777-1782

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cs500167k

Keywords

alloy nanoparticles; tandem reaction; dehydrogenation; hydrogenation; nitro/nitrile compounds; primary amines

Funding

  1. Scientific and Technological Research Council of Turkey (TUBITAK) [113Z276]
  2. U.S. Army Research Laboratory
  3. U.S. Army Research Office under the Multi University Research Initiative (MURI) [W911NF-11-1-0353]

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We report a facile synthesis of monodisperse NiPd alloy nanoparticles (NPs) and their assembly on graphene (G) to catalyze the tandem dehydrogenation of ammonia borane (AB) and hydrogenation of R-NO2 and/or R-CN to R-NH2 in aqueous methanol solutions at room temperature. The 3.4 nm NiPd alloy NPs were prepared by coreduction of nickel(II) acetate and palladium(H) acetlyacetonate by borane-tert-butylamine in oleylamine and deposition on G via a solution phase self-assembly process. G-NiPd showed composition-dependent catalysis on the tandem reaction with G-Ni30Pd70 being the most active. A variety of R-NO2 and/or R-CN derivatives were reduced selectively into R-NH2 via G-Ni30Pd70 catalyzed tandem reaction in 5-30 mm reaction time with the conversion yields reaching up to 100%. Our study demonstrates a new approach to G-NiPd-catalyzed dehydrogenation of AB and hydrogenation of R-NO2 and R-CN. The G-NiPd NP catalyst is efficient and reusable, and the reaction can be performed in an environment-friendly process with short reaction times and high yields.

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