首页> 外文期刊>Organic process research & development >Au Core-Pd Shell Bimetallic Nanoparticles Immobilized within Hyper-Cross-Linked Polystyrene for Mechanistic Study of Suzuki Cross-Coupling: Homogeneous or Heterogeneous Catalysis?
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Au Core-Pd Shell Bimetallic Nanoparticles Immobilized within Hyper-Cross-Linked Polystyrene for Mechanistic Study of Suzuki Cross-Coupling: Homogeneous or Heterogeneous Catalysis?

机译:Au Core-Pd壳双金属纳米粒子固定在超交联聚苯乙烯内,用于铃木交叉偶联的机械研究:均匀或异质催化?

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摘要

The synthesis of catalytically active bimetallic Au-Pd nanoparticles stabilized in hyper-cross-linked polystyrene (HPS) for Suzuki cross-coupling of 4-bromoanisole (4-BrAn) and phenylboronic acid is presented. The core-shell structure with a thin (less than 1 nm) Pd shell and a Au core was proven by X-ray diffraction and high-angle annular dark-field scanning transmission electron microscopy combined with energy-dispersive X-ray spectroscopy. More than a 2-fold increase in 4-BrAn conversion was found in comparison with monometallic Pd/HPS. Moreover, when the Suzuki reaction was carried out under visible-light irradiation, the product yield further increased by about 1.3 times (from 56.1% up to 73.7%). This effect was assigned to a local surface plasmon resonance arising in the Au core that allowed electron transfer to the extremely thin Pd layer due to intimate contact with gold. The results suggest that the rate-limiting step of the catalytic cycle takes place on the surface of the Pd shell, serving as evidence of the heterogeneous catalysis nature.
机译:呈现在4-溴吲哚(4-糠)和苯基硼酸的Suzuki交联中稳定在超交联聚苯乙烯(HPS)中稳定的催化活性双金属Au-Pd纳米颗粒。通过X射线衍射和高角度环形暗场扫描透射电子显微镜与能量分散X射线光谱合并,证明具有薄(小于1nm)Pd壳和Au芯的核壳结构。与单金属Pd / HPS相比,发现了4-Bran转化率增加超过2倍。此外,当在可见光照射下进行铃木反应时,产物产率进一步增加了约1.3倍(从56.1%高达73.7%)。该效果被分配给Au核中产生的局部等离子体共振,其由于与金属与金而接触而允许电子转移到极薄的PD层。结果表明,催化周期的速率限制步骤发生在PD壳表面上,作为异质催化性质的证据。

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