首页> 外文期刊>RSC Advances >Immobilized copper-layered nickel ferrite on acid-activated montmorillonite, [(NiFe2O4@Cu)(H+-Mont)], as a superior magnetic nanocatalyst for the green synthesis of xanthene derivatives
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Immobilized copper-layered nickel ferrite on acid-activated montmorillonite, [(NiFe2O4@Cu)(H+-Mont)], as a superior magnetic nanocatalyst for the green synthesis of xanthene derivatives

机译:在酸活化的蒙脱石上固定化铜层镍铁素体,[(NiFe2O4 @ Cu)],作为X吨衍生物的绿色合成的优质磁性纳米催化剂

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摘要

In this study, the immobilization of copper-layered nickel ferrite on the surface and in the cavities of acid-activated montmorillonite (H+-Mont) was investigated. In this context, magnetic nanoparticles (MNPs) of NiFe2O4 as the prime magnetic cores were prepared. Next, through the reduction of Cu2+ ions with sodium borohydride, the nanoparticles of Cu-0 were immobilized on the nanocore-surface of NiFe2O4, and the constituent NiFe2O4@Cu MNPs were obtained. Moreover, through the activation of montmorillonite K10 (Mont K10) with HCl (4 M) under controlled conditions, the H+-Mont constituent was prepared. The nanostructured NiFe2O4@Cu was then intercalated within the interlayers and on the external surface of the H+-Mont constituent to afford the novel magnetic nanocomposite (NiFe2O4@Cu)(H+-Mont). The prepared clay nanocomposite was characterized using FTIR spectroscopy, SEM, EDX, XRD, VSM and BET analyses. The obtained results showed that through acid-activation, the stacked-sheet structure of Mont K10 was exfoliated to tiny segments, leading to a significant increase in the surface area and total pore volume of the H+-Mont constituent as compared to those of montmorillonite alone. SEM analysis also exhibited that the dispersion of NiFe2O4@Cu MNPs in the interlayers and on the external surface of acid-activated montmorillonite was carried out successfully, and the nanoparticle sizes were distributed in the range of 15-25 nm. The BET surface analysis also indicated that through the immobilization of NiFe2O4@Cu MNPs, the surface area and total pore volume of the H+-Mont system were decreased. The catalytic activity of (NiFe2O4@Cu)(H+-Mont) was further studied towards the synthesis of substituted 13-aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H) tetraones 3(a-k) and 3,3,6,6-tetramethyl-9-aryl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H) diones 5(a-k)via the pseudo-one-pot three-component cyclocondensation of 2-hydroxy-1,4-naphthoquinone (Lawsone)/dimedone and aromatic aldehydes in a mixture of H2O-EtOH (1 : 1 mL) as a green solvent at 80-90 degrees C. The (NiFe2O4@Cu)(H+-Mont) MNPs can be easily separated from the reaction mixture by an external magnetic field and reused for seven consecutive cycles without significant loss of catalytic activity.
机译:在本研究中,研究了研究表面和酸活化的蒙脱石(H + -mont)的表面和空腔中的铜层镍铁氧体的固定。在这种情况下,制备NiFe2O4的磁性纳米颗粒(MNP)作为主要磁芯。接下来,通过用硼氢化钠的Cu 2 +离子的还原,将Cu-0的纳米颗粒固定在NiFe2O4的纳米腔表面上,得到组分NiFe2O4 @ Cu MNP。此外,通过在受控条件下用HCl(4M)的HCl(4M)激活蒙脱石K10(MONT K10),制备H + -MONT成分。然后将纳米结构的NiFe2O4 @ Cu嵌入夹层内和H + -mont成分的外表面上,得到新型磁性纳米复合材料(NiFe2O4 @ Cu)(H + -mont)。使用FTIR光谱,SEM,EDX,XRD,VSM和BET分析表征制备的粘土纳米复合物。得到的结果表明,通过酸激活,将MONT K10的堆叠片结构剥离到微小的段中,与单独的蒙脱石相比,H + -mont成分的表面积和总孔体积显着增加。 SEM分析还表明,成功地进行了NiFe2O4 @ Cu MnP和酸活化的蒙脱石外表面上的分散,纳米颗粒尺寸在15-25nm的范围内分布。 BET表面分析还表明,通过固定NiFe2O4 @ Cu Mnps,H + -mont系统的表面积和总孔体积被降低。进一步研究(NIFE2O4 @ Cu)(H + -mont)的催化活性朝向取代的13-芳基-5H-二苯苯苯苯苯并[B,I] x one-5,7,12,14(13H)Tetraones 3(AK)的合成通过伪一体,和3,3,6,6-四甲基-9-芳基-3,4,5,6,7,9-六羟基-1H- x啶-1,8(2h)脱硫5(ak) - 在80-90摄氏度下,在H 2 O-ETOH(1:1mL)的混合物中,在H 2 O-EtOH(1:1mL)的混合物中,在H 2 O-EtOH(1:1mL)的混合物中进行三分 - 羟基-1,4-萘醌(授权)/ Dimedone和芳香族醛。( NiFe2O4 @ Cu)(H + -mont)Mnps可以通过外部磁场容易地与反应混合物分离,并重复使用七个连续循环,而不会显着损失催化活性。

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    《RSC Advances》 |2019年第48期|共15页
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  • 正文语种 eng
  • 中图分类 化学;
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