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SOH功能化环氧固定化FeO核壳磁性纳米粒子作为一种高效、可重复使用且环保的催化剂用于可持续绿色合成吡喃和吡咯烷酮衍生物

SOH-Functionalized Epoxy-Immobilized FeO Core-Shell Magnetic Nanoparticles as an Efficient, Reusable, and Eco-Friendly Catalyst for the Sustainable and Green Synthesis of Pyran and Pyrrolidinone Derivatives.

作者信息

Kalantari Fatemeh, Esmailipour Hussein, Ahankar Hamideh, Ramazani Ali, Aghahosseini Hamideh, Kaszubowski Oskar, Ślepokura Katarzyna

机构信息

Department of Chemistry, University of Zanjan, Zanjan 45371-38791, Iran.

Department of Chemistry, Abhar Branch, Islamic Azad University, P.O. Box 22, Abhar 45619-33367, Iran.

出版信息

ACS Omega. 2023 Jul 3;8(29):25780-25798. doi: 10.1021/acsomega.3c01068. eCollection 2023 Jul 25.

Abstract

A SOH-functionalized epoxy-immobilized FeO core-shell magnetic nanocatalyst was prepared through a simple three-step procedure, and it was identified by various analyses such as Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), differential thermal gravity (DTG), Brunauer-Emmett-Teller (BET) analysis, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), vibration sample magnetometry (VSM), and powder X-ray diffraction (PXRD). BET analysis showed that the as-prepared nanocatalyst was synthesized with a mesoporous structure and high specific area (35.45 m g). The TEM image clearly showed that the particle size distribution was in the range of 47-65 nm. The designed magnetic nanocatalyst was used successfully in the synthesis of pyran derivatives via the reaction of dimedone, malononitrile, and various aromatic aldehydes and synthesis of pyrrolidinone derivatives via the reaction of various aromatic aldehydes, aniline, and diethyl acetylenedicarboxylate. The nanocatalyst was simply isolated from the reaction mixture utilizing an external magnet and reused several times according to the model reactions without significant loss in its efficiency.

摘要

通过一个简单的三步程序制备了一种SOH功能化的环氧固定化FeO核壳磁性纳米催化剂,并通过傅里叶变换红外(FT-IR)光谱、扫描电子显微镜(SEM)、差示热重(DTG)、布鲁诺尔-埃米特-泰勒(BET)分析、透射电子显微镜(TEM)、能量色散X射线光谱(EDX)、热重分析(TGA)、振动样品磁强计(VSM)和粉末X射线衍射(PXRD)等各种分析对其进行了鉴定。BET分析表明,所制备的纳米催化剂具有介孔结构和高比表面积(35.45 m²/g)。TEM图像清楚地表明,粒径分布在47-65 nm范围内。所设计的磁性纳米催化剂成功用于通过二氢嘧啶酮、丙二腈和各种芳香醛的反应合成吡喃衍生物,以及通过各种芳香醛、苯胺和二乙基乙炔二羧酸酯的反应合成吡咯烷酮衍生物。利用外部磁铁可将纳米催化剂简单地从反应混合物中分离出来,并根据模型反应重复使用多次,其效率不会有明显损失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd38/10373207/2063caca561f/ao3c01068_0002.jpg

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