首页> 外文期刊>Advanced synthesis & catalysis >Air-Stable and Highly Active Dendritic Phosphine Oxide-Stabilized Palladium Nanoparticles;Preparation,Characterization and Applications in the Carbon-Carbon Bond Formation and Hydrogenation Reactions
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Air-Stable and Highly Active Dendritic Phosphine Oxide-Stabilized Palladium Nanoparticles;Preparation,Characterization and Applications in the Carbon-Carbon Bond Formation and Hydrogenation Reactions

机译:稳定的高活性树枝状膦氧化物稳定的钯纳米粒子;制备,表征及在碳-碳键形成及氢化反应中的应用

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Dendrimer-stabilized palladium nanoparticles were formed in the reduction of palldium bis-(acetylacetonate)[Pd(acac)2]in the presence of phosphine dendrimer ligands using hydrogen in tet-rahydrofuran.The resulting Pd nanoparticles were characterized by TEM,~(31)PNMR and ~(31)P MAS NMR.The results indicated that the dendritic phosphine ligands were oxidized to phosphine oxides.These dendrimer-stabilized Pd nanoparticles were demonstrated to be efficient catalysts for Suzuki and Stille coupling reactions and hydrogenations.The dendritic wedges served as a stabilizer for keeping the nanoparticles from aggregating,and as a vehicle for facilitating the separation and/or the recycling of the Pd catalyst.In the case of the Suzuki coupling re-action,these Pd nanoparticles exhibited high catalytic efficiency(TON up to 65,000)and air stability as compared with the commonly used homogeneous catalyst tetrakis(triphenylphosphine)palladium[Pd-(PPh3)4].In addition,the results obtained from the bulky dendritic substrate suggest that the Pd nanoparticles might act as reservoir of catalytically active species,and that the reaction is actually catalyzed by the soluble Pd(0)and/or Pd(II)species leached from the nanoparticle surface.
机译:在四氢呋喃-呋喃中使用氢在膦类树枝状大分子配体存在下还原双-(乙酰丙酮)钯[Pd(acac)2],形成了树枝状聚合物稳定的钯纳米颗粒。通过TEM对所得Pd纳米颗粒进行表征,〜(31结果表明,树状大分子稳定的Pd纳米粒子是Suzuki和Stille偶联反应和加氢的有效催化剂。作为防止纳米粒子聚集的稳定剂,以及作为促进Pd催化剂分离和/或再循环的载体。在Suzuki偶联反应的情况下,这些Pd纳米粒子具有很高的催化效率(TON至与常用的均相催化剂四(三苯基膦)钯[Pd-(PPh3)4]相比,空气稳定性更高,达到了65,000)和空气稳定性。树突状基质表明,Pd纳米颗粒可能充当催化活性物质的储存库,并且该反应实际上是由从纳米颗粒表面浸出的可溶性Pd(0)和/或Pd(II)物种催化的。

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