新型生物相容性核/壳结构FeO@NFC@Co(ii)作为多组分反应中的新型催化剂:一种在水介质中一锅法合成4-吡喃和吡喃并吡唑的高效可持续方法及新型可重复使用材料
Novel biocompatible core/shell FeO@NFC@Co(ii) as a new catalyst in a multicomponent reaction: an efficient and sustainable methodology and novel reusable material for one-pot synthesis of 4-pyran and pyranopyrazole in aqueous media.
作者信息
Kargar Pouya Ghamari, Bagherzade Ghodsieh, Eshghi Hossein
机构信息
Department of Chemistry, Faculty of Sciences, University of Birjand Birjand 97175-615 Iran
Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad Mashhad Iran.
出版信息
RSC Adv. 2020 Oct 8;10(61):37086-37097. doi: 10.1039/d0ra04698a. eCollection 2020 Oct 7.
Today, due to the developing need for inexpensive catalysts, recyclable magnetic nanocatalysts immobilized on polysaccharides possess many advantages over classical heterogeneous catalysts. However, cellulose has been an appealing material in catalysis science and technology. In this work, by controlling the interaction between the inorganic complexes and the support material, we designed a high activity nanostructured combination of a magnetic nanoparticle FeO@NFC@Co(ii) terminated complex as a multi-nuclear catalyst. This protocol involves an environment friendly approach using cobalt acetate. The magnetic nanostructure FeO@NFC@Co(ii) can be used as a novel, green, and a powerful catalyst that demonstrates a short reaction time, high yield and easy procedure for the cascade Knoevenagel-Michael-cyclocondensation reaction for the one-pot synthesis of 4-pyrans and pyranopyrazoles. The superparamagnetic nanocomposite could be conveniently separated by using an external magnet. Moreover, the catalyst could be reused at least five times in new reaction runs without a noticeable loss of activity. The prepared catalyst was characterized by FT-IR, XRD, VSM, FESEM, EDAX, TEM, ICP, and TGA techniques. The experiments were achieved with good yields and implied that the catalytic method was effective and convenient for heterocyclic synthesis.
如今,由于对廉价催化剂的需求不断增加,固定在多糖上的可回收磁性纳米催化剂比传统的多相催化剂具有许多优势。然而,纤维素在催化科学与技术领域一直是一种有吸引力的材料。在这项工作中,通过控制无机配合物与载体材料之间的相互作用,我们设计了一种高活性的纳米结构组合,即磁性纳米颗粒FeO@NFC@Co(ii)端基配合物作为多核催化剂。该方案涉及使用醋酸钴的环境友好方法。磁性纳米结构FeO@NFC@Co(ii)可作为一种新型、绿色且高效的催化剂,在一锅法合成4-吡喃和吡喃并吡唑的串联Knoevenagel-迈克尔-环缩合反应中表现出反应时间短;产率高和操作简便的特点。超顺磁性纳米复合材料可以通过使用外部磁铁方便地分离。此外,该催化剂在新的反应运行中可以重复使用至少五次,而活性没有明显损失。通过FT-IR、XRD、VSM、FESEM、EDAX、TEM、ICP和TGA技术对制备的催化剂进行了表征。实验获得了良好的产率,表明该催化方法对于杂环合成是有效且方便的。
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