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首页> 外文期刊>Journal of inorganic and organometallic polymers and materials >Tannic Acid-Functionalized Silica Coated Fe_3O_4 Nanoparticles as a Novel and Magnetically Separable Catalyst for Green Synthesis of Aryl Naphtho[1,3]Oxazine-2-Thiones
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Tannic Acid-Functionalized Silica Coated Fe_3O_4 Nanoparticles as a Novel and Magnetically Separable Catalyst for Green Synthesis of Aryl Naphtho[1,3]Oxazine-2-Thiones

机译:单宁酸官能化二氧化硅涂覆的Fe_3O_4纳米粒子作为新型和磁性可分离的催化剂,用于绿色合成芳基萘硫醚[1,3]恶唑-2-张

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摘要

Tannic acid-functionalized silica-coated Fe(3)O(4)nanoparticles (Fe3O4@SiO2@Tannic acid) 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 (EDS). Fe3O4@SiO2@Tannic acid supply an environmentally friendly procedure for the synthesis of 1,3-oxazine-2-thiones through three-component grinding reaction of various aldehydes, thiourea, and alpha-naphthol or beta-naphthol in accordance with green chemistry rules. In the other study, this novel synthesized magnetically reusable catalyst was introduced as a new avenue for the synthesis of Aryl naphtho[1,3]oxazine-2-thione using the reaction between synthetized azo-linked aldehydes, malononitrile, and phenylhydrazine orp-tolylhydrazine. 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(1)H NMR,C-13 NMR and FTIR spectral data and elemental analyses.
机译:单宁酸官能化二氧化硅涂层Fe(3)O(4)纳米颗粒(Fe3O4 @ SiO 2鞣酸)合成,并通过透射电子显微镜(TEM),场发射扫描电子显微镜(FE-SEM),傅里叶变换红外线光谱学(FT-IR),振动样品磁体(VSM),X射线粉末衍射(XRD)和X射线光谱(EDS)。 Fe3O4 @ SiO 2 @鞣酸酸提供环保程序,用于通过各种醛,硫脲和α-萘酚或β-萘酚的三组分研磨反应合成1,3-氧碱-2-酮,根据绿色化学规则。在另一种研究中,将该新颖的合成的磁性可重复使用的催化剂作为合成芳基[1,3]恶唑-2-酮的新途径,使用合成的偶氮连接的醛,丙二腈和苯基肼或苯甲酸苯甲酰肼之间的反应。这些化合物以高产率和短反应时间得到。可以容易地回收催化剂并重用六个周期,几乎一致的活性。通过(1)H NMR,C-13 NMR和FTIR光谱数据和元素分析证实了合成芳基萘烷[1,3]恶氨酸-2-Thione化合物的结构。

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