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Ce@STANPs/ZrO2 as Nanocatalyst for MulticomponentSynthesis of Isatin-Derived Imidazoles under Green Reaction Conditions

机译:Ce @ STANPs / ZrO2作为多组分纳米催化剂绿色反应条件下合成Isatin衍生的咪唑

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摘要

A highly efficient and recyclable catalyst, cerium-immobilized silicotungstic acid nanoparticle-impregnated zirconia (Ce@STANPs/ZrO2), has been synthesized. The catalytic activity of Ce@STANPs/ZrO2 was investigated for the first time in multicomponent synthesis of isatin-based imidazoles under microwave irradiation in water. Ce@STANPs/ZrO2 was used for C=O bond activation in overall reaction to synthesize isatin-based imidazoles. The structure of catalyst was confirmed by characterization techniques, such as Fourier transform infrared (FTIR), scanning electron microscopy (SEM)/energy dispersive X-ray, elemental mapping, transmission electron microscopy, ζ-potential and diffraction light scattering, X-ray diffraction (XRD), thermogravimetric analysis, temperature-programmed desorption-NH3, electron paramagnetic resonance (EPR), and inductively coupled plasma atomic emission spectroscopy (ICP-AES) analyses. The recovered catalyst was found to be efficient up to seventh cycle and was confirmed by FTIR, SEM, XRD, EPR, and ICP-AES analyses. The advantages of the present protocol are recyclability of catalyst, green reaction conditions, excellent yield (94%) of the products, shorter reaction time period (5–7 min), and clean reaction profile.
机译:合成了一种高效且可循环利用的催化剂,铈固定化硅钨酸纳米粒子浸渍的氧化锆(Ce @ STANPs / ZrO2)。在水中微波辐射下,首次研究了Ce @ STANPs / ZrO2在多组分合成基于isatin的咪唑中的催化活性。 Ce @ STANPs / ZrO2在整个反应中用于C = O键活化,以合成基于isatin的咪唑。催化剂的结构通过表征技术得到证实,例如傅立叶变换红外(FTIR),扫描电子显微镜(SEM)/能量色散X射线,元素图谱,透射电子显微镜,ζ势和衍射光散射,X射线衍射(XRD),热重分析,程序升温脱附NH3,电子顺磁共振(EPR)和电感耦合等离子体原子发射光谱(ICP-AES)分析。发现回收的催化剂在第七个循环之前都是有效的,并通过FTIR,SEM,XRD,EPR和ICP-AES分析得到了证实。本方案的优点是催化剂的可回收性,绿色反应条件,优异的产物收率(94%),较短的反应时间(5-7分钟)和干净的反应曲线。

著录项

  • 期刊名称 ACS Omega
  • 作者单位
  • 年(卷),期 2018(3),8
  • 年度 2018
  • 页码 10357–10364
  • 总页数 8
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

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