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A green synthesis of spirooxindole derivatives catalyzed by SiO2@g-C3N4 nanocomposite

机译:SiO2催化的螺氧吲哚衍生物的绿色合成 - G-C3N4纳米复合材料

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In this study, SiO2 nanoparticles were immobilized onto the surface of g-C3N4 nanosheets. The characterization of SiO2@g-C3N4 nanocomposite has been done by Fourier transform infrared spectra, X-ray diffraction, thermo-gravimetric analysis, scanning electron microscopy and transmission electron microscopy. The one-pot synthesis of spirooxindole derivatives was investigated via C-C bond formation reaction in the presence of a catalytic amount of SiO2@g-C3N4 nanocomposite using isatin (1 mmol), dimedone (1 mmol) and malononitrile (1 mmol) at ambient temperature in EtOH/water (1:1) media and the corresponding products were synthesized in excellent yields (90-95%) in short time (3-5 min). 4-Hydroxycoumarin was also subjected to the reaction instead of 1,3-diketones under similar conditions and the reactions proceeded in a longer time than for 1,3-diketones (8-11 min) with the products being obtained in 87-95% yields. The advantages of this catalyst include mild reaction conditions, a green and inexpensive nanocatalyst and green media. The nanocomposite was reused several times and applied in the next run without loss of reactivity.
机译:在该研究中,将SiO2纳米颗粒固定在G-C3N4纳米片的表面上。 SiO2 @ G-C3N4纳米复合材料的表征已通过傅里叶变换红外光谱,X射线衍射,热重分析,扫描电子显微镜和透射电子显微镜完成。通过在环境温度下在环境温度下在催化量的SiO 2 -C 3 -C3N4纳米复合材料的情况下通过Cc键形成反应研究螺氧吲哚衍生物的单罐合成。在环境温度下在EtOH /水(1:1)中,在短时间内以优异的产率(90-95%)合成相应的产物(3-5分钟)。在类似条件下,还对反应而不是1,3-二酮进行反应,并在较长的时间内进行的反应比1,3-二酮(8-11分钟)在87-95%中获得的产品产量。该催化剂的优点包括温和的反应条件,绿色和廉价的纳米催化剂和绿色培养基。将纳米复合材料重复使用数次并在下一次运行中施用而不会损失反应性。

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