首页> 外文期刊>Catalysis Letters >Novel Cu(0)-Fe3O4@SiO2/NH(2)cel as an Efficient and Sustainable Magnetic Catalyst for the Synthesis of 1,4-Disubstituted-1,2,3-triazoles and 2-Substituted-Benzothiazoles via One-Pot Strategy in Aqueous Media
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Novel Cu(0)-Fe3O4@SiO2/NH(2)cel as an Efficient and Sustainable Magnetic Catalyst for the Synthesis of 1,4-Disubstituted-1,2,3-triazoles and 2-Substituted-Benzothiazoles via One-Pot Strategy in Aqueous Media

机译:新型Cu(0)-Fe3O4 @ SiO2 / NH(2)cel作为一种高效,可持续的磁催化剂,用于通过一锅法合成1,4-二取代-1,2,3-三唑和2-取代的苯并噻唑在水介质中

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摘要

A novel, air stable, water dispersible and efficient magnetic catalyst based on copper nanoparticles onto ethylene diamine functionalized inorganic/organic composite [Cu(0)-Fe3O4@SiO2/NH(2)cel] has been prepared. Functionalization of inorganic/organic composite by ethylene diamine imparts desirable chemical functionality and enables the generation of active sites for the immobilization of Cu(0) nanoparticles. The novel catalyst system has been well characterized by various techniques like FTIR, TGA, XRD, SEM, HRTEM, EDX, ICP-AES, UV-Vis and VSM. Further, Cu(0)-Fe3O4@SiO2/NH(2)cel opens up a new avenue to introduce a very useful and efficient catalytic system for the one-pot synthesis of 1,4-disubstituted-1,2,3-triazoles via 1,3-dipolar cycloaddition of terminal acetylenes to azides, generated in situ from anilines in water at room temperature, and one-pot three component reaction of 2-iodoaniline, aldehyde and thiourea as sulphur source for the synthesis of 2-substituted-benzothiazole derivatives in water. The novel heterogeneous magnetic catalyst offers recyclability without significant deterioration in catalytic activity and can be easily recovered using an external magnet, thus making it eco-friendly and economical to perform the desired transformations.
机译:制备了一种基于铜纳米粒子在乙二胺官能化的无机/有机复合物[Cu(0)-Fe3O4 @ SiO2 / NH(2)cel]上的新型,空气稳定,水分散性和高效的磁性催化剂。乙二胺对无机/有机复合物的官能化赋予所需的化学官能度,并能够生成用于固定Cu(0)纳米粒子的活性位。该新型催化剂体系已通过多种技术进行了很好的表征,例如FTIR,TGA,XRD,SEM,HRTEM,EDX,ICP-AES,UV-Vis和VSM。此外,Cu(0)-Fe3O4 @ SiO2 / NH(2)cel开辟了一条新途径,为一锅法合成1,4-二取代-1,2,3-三唑引入了非常有用和高效的催化体系通过在室温下由水中苯胺原位生成的末端乙炔与叠氮化物的1,3-偶极环加成反应以及2-碘苯胺,醛和硫脲作为硫源的一锅三组分反应来合成2-取代的-水中的苯并噻唑衍生物。新型多相磁性催化剂提供了可回收性,而催化活性没有显着降低,并且可以使用外部磁体轻松回收,从而使其环保且经济地进行所需的转化。

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