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首页> 外文期刊>ACS Sustainable Chemistry & Engineering >Monodisperse Ni@Pd Core@Shell Nanoparticles Assembled on Reduced Graphene Oxide as a Highly Efficient and Reusable Heterogeneous Catalyst for the C-H Bond Arylation of Imidazo[1,2-a]pyridine with Aryl Halides
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Monodisperse Ni@Pd Core@Shell Nanoparticles Assembled on Reduced Graphene Oxide as a Highly Efficient and Reusable Heterogeneous Catalyst for the C-H Bond Arylation of Imidazo[1,2-a]pyridine with Aryl Halides

机译:单分散Ni @ Pd核心@壳纳米粒子在将石墨烯氧化物的还原氧化物上组装为高效且可重复使用的非均相催化剂,用于咪唑的C-H键合芳基与芳基卤化物的C-H键芳基化

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摘要

We report herein, for the first time, the direct C-H bond arylation of imidazo[1,2-a]pyridine with aryl halides using monodisperse Ni@Pd core@shell nanoparticles assembled on reduced graphene oxide (rGO) as a highly efficient and reusable heterogeneous catalyst. Monodisperse Ni@Pd core@shell nanoparticles (NPs) were synthesized by using one-pot successive reduction of metal precursors in the presence of oleylamine and trioctyl phosphine and then assembled on rGO via a liquid-phase self-assembly method to yield rGO-Ni@Pd nanocatalyst. The structures of the colloidal Ni@Pd core@shell NPs and rGO-Ni@Pd nano catalyst were characterized by TEM, high-resolution TEM (HR-TEM), STEM-EDS, XPS, and ICP-MS. Next, rGO-Ni@Pd nanocatalysts as well as rGO-Ni and rGO-Pd counterparts were first tested in the direct C-H bond arylation of imidazo[1,2-a]pyridine with bromobenzene under tunable reaction conditions to find the optimum reaction conditions. Under the optimum reaction conditions, the substrate scope of rGO-Ni@Pd-catalyzed direct C-H arylation of irnidazo[1,2-a]pyridine was examined by performing the catalytic reactions with a variety of aryl halides. These studies showed for the first time that rGO-Ni@Pd nanocatalysts are highly efficient and reusable catalysts in the direct C-H bond arylation reactions and have a high potential to be applied in other C-H activation reactions.
机译:我们在本文中报告了咪唑[1,2-a]吡啶的直接CH键芳基,使用芳基卤化物使用单分散的Ni核心/壳纳米颗粒组装在氧化物氧化物(RGO)上组装为高效且可重复使用异质催化剂。通过在油胺和三辛基膦的存在下使用单盆连续减少金属前体,通过液相自组装方法在RGO上组装在RGO上,通过使用单盆连续减少金属前体,通过液相自组装方法在RGO上组装,得到单位的NI核心@壳纳米粒子(NPS),以产生RGO-Ni @PD纳米催化剂。胶体Ni @ Pd核心@ Shell NPS和RGO-Ni @ Pd纳米催化剂的结构特征在于TEM,高分辨率TEM(HR-TEM),茎EDS,XPS和ICP-MS。接下来,在可调节反应条件下,首先在可调节反应条件下在咪唑[1,2-a]吡啶的直接CH键芳基的直接CH键芳基的直接CH键芳基和RGO-Ni和RGO-Pd对应物中的rgo-Ni和Rgo-Pd对应物。找到最佳反应条件。在最佳反应条件下,通过用各种芳基卤化物进行催化反应,检查rgo-Ni @ Pd催化直接C-H芳啶的rgo-Ni @ Pd催化直接C-H芳啶的底物范围。这些研究首次显示RGO-Ni @ Pd纳米催化剂在直接C-H键芳基化反应中具有高效且可重复使用的催化剂,并且具有高潜力才能在其它C-H激活反应中应用。

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