以1,3,5-三(2-羟乙基)异氰脲酸酯和硼酸为官能团的新型高效磁性纳米催化剂,用于合成对称和不对称汉奇酯

M. Sam, M. Dekamin
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引用次数: 0

摘要

设计了一种以1,3,5-三(2-羟乙基)异氰脲酸酯和硼酸(Fe3O4/SiO2/CPTS/THEIC/(CH2)3B(OH)2)为官能团的新型磁核/壳纳米催化剂(Fe3O4/SiO2/CPTS/THEIC/(CH2)3B(OH)2)为官能团),并采用傅里叶变换红外(FTIR)光谱、氮吸附-解吸技术(BET)、热重分析(TGA)和x射线衍射(XRD)、振动样品磁强计(VSM)、场发射扫描电镜(FESEM)和能量色散x射线(EDX)光谱对其进行了表征。研究了Fe3O4/SiO2/CPTS/THEIC/(CH2)3B(OH)2作为高效磁可回收催化剂,在回流条件下,以乙乙酸乙酯和/或二美酮、不同醛类和乙酸铵为原料,进行一锅多组分反应合成聚氢喹啉(PHQs)和聚氢吖啶(PHAs)的催化活性。该绿色方案的显著优点是,所需phq或pha产品的高定量收率,底物范围广,消除了任何有毒重金属或用于修饰催化剂的腐蚀性试剂,简单的加工程序,短的反应时间和低的催化剂负载。这种磁性纳米颗粒催化剂的另一个优点是它能够在随后的六次运行中轻松地从反应混合物中分离和回收,而不会显著损失其催化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel and efficient magnetic nanocatalyst functionalized with 1,3,5-tris(2-hydroxyethyl)isocyanurate and boric acid for the synthesis of symmetric and asymmetric Hantzsch esters
A new magnetic core/shell nanocatalyst functionalized with 1,3,5-tris(2-hydroxyethyl)isocyanurate and boric acid (Fe3O4/SiO2/CPTS/THEIC/(CH2)3B(OH)2) was designed and properly characterized by the Fourier transform infrared (FTIR) spectroscopy, nitrogen adsorption–desorption technique (BET), thermal gravimetric analysis (TGA) and X-ray diffraction (XRD), vibrating sample magnetometer (VSM), field emission scanning electron microscopy (FESEM) and energy-dispersive X-ray (EDX) spectroscopy. The catalytic activity of Fe3O4/SiO2/CPTS/THEIC/(CH2)3B(OH)2, as an efficient magnetically recoverable catalyst, was investigated for the synthesis of polyhydroquinolines (PHQs) as well as polyhydroacridines (PHAs) via one-pot multicomponent reactions of ethyl acetoacetate and / or dimedone, different aldehydes and ammonium acetate in EtOH under reflux conditions. High to quantitative yields of the desired PHQs or PHAs products, wide scope of the substrates, eliminating of any toxic heavy metals or corrosive reagents for modification of the catalyst, simple work-up procedure, short reaction times and low loading of the catalyst are remarkable advantages of this green protocol. An additional advantage of this magnetic nanoparticles catalyst is its ability to be separated and recycled easily from the reaction mixture with minimal efforts in six subsequent runs without significant loss of its catalytic activity.
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