首页> 美国卫生研究院文献>ACS Omega >Design and Exploration of Catalytic Activity of Two-DimensionalSurface-Engineered Graphene Oxide Nanosheets in the Transannulationof N-Heterocyclic Aldehydes or Ketones with Alkylamines
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Design and Exploration of Catalytic Activity of Two-DimensionalSurface-Engineered Graphene Oxide Nanosheets in the Transannulationof N-Heterocyclic Aldehydes or Ketones with Alkylamines

机译:二维催化活性的设计与探索表面工程氧化石墨烯纳米片的转环烷基胺与N-杂环醛或酮的合成

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摘要

In this work, pharmaceutically and biologically important compounds containing imidazo[1,5-a]pyridine nuclei have been synthesized via transannulation of N-heteroaryl aldehydes or ketones with alkylamines using a graphene oxide-supported copper catalyst. The nanocatalyst was fabricated by the covalent immobilization of 4-aminoantipyrine onto an amine-functionalized graphene oxide nanosupport followed by its metallation with copper acetate. Structural analysis by transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy (XPS), and X-ray diffraction demonstrates that the two-dimensional sheet-like structure of graphene oxide is maintained even after the chemical modifications, whereas XPS revealed crucial information related to elemental composition and surface electronic states of the metal present in the catalyst. Apart from this, Fourier transform infrared spectroscopy helped in identifying the degree of oxidation and the presence of oxygenated groups in graphene oxide nanocomposites. As a heterogeneous catalyst, this graphene oxide-supportedcopper complex showed moderate to good catalytic activity in the C(sp3)–H bond activation/amination of a variety of substrates.This superior catalytic performance originated from the unique 2-dimensionalstructure of graphene oxide-based material which provided space betweengraphitic overlayers due to appropriate positioning of metal on theirbasal planes, decreasing the diffusion resistances of reactant surfaces,thus making it function as a nanoreactor. More importantly, this nanomaterialcould be recovered easily and reused repeatedly by simple washingwithout chemical treatment with no appreciable loss in its catalyticactivity, showing good potential for increasing the overall turnovernumber of this synthetically useful catalyst.
机译:在这项工作中,通过使用氧化石墨烯负载的铜催化剂,将N-杂芳基醛或酮与烷基胺进行反环合成,合成了包含咪唑并[1,5-a]吡啶核的药学和生物学上重要的化合物。通过将4-氨基安替比林共价固定在胺官能化的氧化石墨烯纳米载体上,然后将其与乙酸铜金属化来制备纳米催化剂。通过透射电子显微镜,扫描电子显微镜,X射线光电子能谱(XPS)和X射线衍射进行的结构分析表明,即使经过化学修饰,氧化石墨烯的二维片状结构也得以保持,而XPS显示出至关重要的作用。与催化剂中存在的金属的元素组成和表面电子态有关的信息。除此之外,傅立叶变换红外光谱有助于确定氧化程度和氧化石墨烯纳米复合材料中氧化基团的存在。作为多相催化剂,该氧化石墨烯负载铜配合物在各种底物的C(sp 3 )– H键活化/胺化反应中显示出中等至良好的催化活性。这种卓越的催化性能源自独特的二维氧化石墨烯基材料之间的结构石墨覆盖层是由于金属在其上的适当位置基面,降低了反应物表面的扩散阻力,因此使其具有纳米反应器的功能。更重要的是,这种纳米材料可以很容易地回收并通过简单的洗涤重复使用无需化学处理,催化活性也没有明显损失活动,显示出增加整体营业额的良好潜力这种合成有用的催化剂的数量。

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