γ-Fe2O3纳米颗粒的合成及叠氮化物-炔环加成反应的催化活性

A. Kumar, K. Sudhakara, B. P. Kumar, A. Raghavender, S. Ravi, Dunkana Negussa Keniec, Yong‐Ill Lee
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引用次数: 6

摘要

近年来,铁纳米颗粒由于其独特的性能、低廉的制备成本以及在铁磁流体、磁光、催化、药物输送系统、磁共振成像和生物学等领域的广泛应用,引起了人们的广泛关注。本研究采用简单共沉淀法合成γ - fe2o3nps,然后在300℃下热处理2小时。在我们的合成路线中,FeCl3和FeCl2作为前体合成了γ-Fe2O3NPs。这种方法既有效又经济。采用x射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、扫描电镜(SEM)、透射电镜(TEM)和振动样品磁强计(VSM)对γ-Fe2O3NPs进行了表征。XRD和FT-IR分析结果表明,合成了γ-Fe2O3NPs。SEM和TEM分析表明,制备的γ-Fe2O3纳米粉体的粒径在11 ~ 13 nm之间。磁滞回线表明,γ-Fe2O3 NPs具有超顺磁性。将合成的γ-Fe2O3NPs应用于叠氮-炔环加成反应合成单三唑。关键词:γ-Fe2O3纳米颗粒;
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of γ-Fe2O3 Nanoparticles and Catalytic activity of Azide-Alkyne Cycloaddition Reactions
Iron nanoparticles (NPs), due to their interesting properties, low cost preparation and many potential applications in ferrofluids, magneto-optical, catalysis, drug delivery systems, magnetic resonance imaging, and biology, have attracted a lot of interest during recent years. In this research, γFe2O3NPs were synthesized through simple co-precipitation method followed by thermal treatment at 300 °C for 2 hours. In our synthesis route, FeCl3 and FeCl2 were employed as precursors to synthesize γ-Fe2O3NPs. This approach is very effective and economical. The γ-Fe2O3NPs were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM),and vibrating sample magnetometer (VSM). The XRD and FT-IR results indicated the formation of γ-Fe2O3NPs. The SEM and TEM images contributed to the analysis of particle size and revealed that the γ-Fe2O3 particle size of the nanopowders ranged from 11 and 13 nm. Magnetic property was measured by VSM at room temperature and hysteresis loops exhibited that the γ-Fe2O3 NPs were super-paramagnetic. The synthesized γ-Fe2O3NPs were applied in order to synthesize mono-triazoles within one molecule using azide-alkyne cycloaddition reactions. KEYWORDS: γ-Fe2O3 Nanoparticles,
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