NiFe 2O 4@Sio 2 nPr@Glucose Amine Nanoparticles as a Green and Magnetically Separable Catalyst for the Grinding Synthesis of Aryl Naphtho[1,3]Oxazine-2-Thiones

M. Nikpassand, Shokoufeh Azmoudeh
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Abstract

Glucose amine‐functionalized silica‐coated NiFe2O4 nanoparticles (NiFe2O4@Sio2nPr@glucose amine) were synthesized and characterized by transmission electron microscope (TEM), Field emission scanning electron microscope (FE-SEM), fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometry (VSM), X-ray powder diffraction (XRD) and X-ray spectroscopy (EDX).  NiFe2O4@SiO2nPr@glucose amine supply an eco-friendly procedure for the synthesis of 1,3-oxazine-2-thiones through three-component grinding reaction of various aldehydes, thiourea, and α-naphthol or β-naphthol in accordance with green chemistry rules. These compounds were obtained in high yields and short reaction times. The catalyst could be easily recovered and reused for six cycles with almost consistent activity. The structures of the synthesized Aryl naphtho[1,3]oxazine-2-thione compounds were confirmed by 1H NMR, 13C NMR and FTIR spectral data and elemental analyses.
NiFe 2O 4@Sio 2 nPr@Glucose纳米胺作为研磨合成芳基萘[1,3]恶嗪-2-硫酮的绿色磁性可分离催化剂
合成了葡萄糖胺功能化二氧化硅包覆的NiFe2O4纳米粒子(NiFe2O4@Sio2nPr@葡萄糖胺),并通过透射电镜(TEM)、场发射扫描电镜(FE-SEM)、傅里叶变换红外光谱(FT-IR)、振动样品磁强计(VSM)、x射线粉末衍射(XRD)和x射线能谱(EDX)对其进行了表征。NiFe2O4@SiO2nPr@葡萄糖胺根据绿色化学规则,通过各种醛、硫脲和α-萘酚或β-萘酚的三组分研磨反应,提供了一种合成1,3-恶嗪-2-硫酮的环保工艺。这些化合物产率高,反应时间短。该催化剂易于回收,可重复使用6次,且活性基本一致。合成的芳基萘[1,3]恶嗪-2-硫酮化合物的结构通过1H NMR、13C NMR、FTIR光谱数据和元素分析得到了证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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