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负载于二氧化硅包覆的杂化锰掺杂钴铁氧体纳米颗粒上的锌络合物作为催化剂用于合成2-氨基-4-吡喃和N-芳基喹啉衍生物。

Zn complexed on hybrid manganese doped cobalt ferrite nanoparticles covered by silica as a catalyst in the synthesis of 2-amino-4-pyran and N- arylquinoline derivatives.

作者信息

Ahadi Najmieh, Mobinikhaledi Akbar, Ebrahimi Amir Hossain

机构信息

Department of Chemistry, Faculty of Science, Arak University, Arak, 38156-88138, Iran.

Institute of Nanosciences and Nanotechnology, Arak University, Arak, Iran.

出版信息

Heliyon. 2024 May 6;10(9):e30620. doi: 10.1016/j.heliyon.2024.e30620. eCollection 2024 May 15.

Abstract

In the present work, Zn complexed on hybrid manganese doped cobalt ferrite nanoparticles covered by silica were synthesized. These MNPs were characterized using different techniques including Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction analysis (XRD), Field emission-scanning electron micro-scope (FE-SEM), Energy-dispersive X-ray spectroscopy (EDS), Vibration sample magnetometer (VSM), Inductively coupled plasma atomic emission spectroscopy (ICP), Zeta potential and Thermogravimetric analysis (TGA). FE-SEM Images showed uniform spherical shape with rough surfaces and an aggregation in structure of MNPs. A decrease in Ms is visible in VSM analysis due to the increase in particle diameter as a result of loading the organic coating on the surface of the magnetic nanoparticles. According to TGA analysis, the synthesized MNPs have good stability up to 125 °C. The ICP analysis indicates the presence of 0.13 mmol/g zinc on the surface of loaded MNPs. The effect of these prepared MNPs as a catalyst was studied in the synthesis of 2-amino-4-pyran and N- arylquinoline derivatives. This method provides excellent yield of products with short reaction time, simple purification and easy separation of the catalyst. Furthermore, the reusability of the catalyst during five periods was not associated with a significant decrease in its activity.

摘要

在本工作中,合成了包覆有二氧化硅的杂化锰掺杂钴铁氧体纳米颗粒上络合锌的产物。使用不同技术对这些磁性纳米颗粒进行了表征,包括傅里叶变换红外光谱(FT-IR)、X射线衍射分析(XRD)、场发射扫描电子显微镜(FE-SEM)、能量色散X射线光谱(EDS)、振动样品磁强计(VSM)、电感耦合等离子体原子发射光谱(ICP)、zeta电位和热重分析(TGA)。FE-SEM图像显示磁性纳米颗粒呈均匀球形,表面粗糙且结构中有团聚现象。由于在磁性纳米颗粒表面负载有机涂层导致粒径增大,VSM分析中可见饱和磁化强度(Ms)降低。根据TGA分析,合成的磁性纳米颗粒在高达125℃时具有良好的稳定性。ICP分析表明负载的磁性纳米颗粒表面存在0.13 mmol/g锌。研究了这些制备的磁性纳米颗粒作为催化剂在合成2-氨基-4-吡喃和N-芳基喹啉衍生物中的作用。该方法能以短反应时间提供优异的产物收率,催化剂的纯化简单且易于分离。此外,催化剂在五个循环中的可重复使用性与其活性的显著降低无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a79/11098855/43ef870e86a4/sc1.jpg

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