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Development of the catalytic reactivity of an oxo-peroxo Mo(VI) Schiff base complex supported on supermagnetic nanoparticles as a reusable green nanocatalyst for selective epoxidation of olefins

机译:超磁性纳米粒子上负载的氧-过氧Mo(VI)Schiff碱配合物作为烯烃选择性环氧化的可重用绿色纳米催化剂的催化反应性的开发

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摘要

A novel ancillary branch coated oxo-peroxo Mo(VI) tetradentate Schiff base complex on superparamagnetic nanoparticles was prepared and characterized by IR spectroscopy, X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), diffuse reflectance spectra (DRS) and atomic absorption spectroscopy (AAS). The catalyst was used for the selective epoxidation of cyclooctene, cyclohexene, styrene, indene, alpha-pinene, 1-hepten, 1-octene, 1-dodecen and trans-stilben using tert-butyl hydroperoxide as an oxidant in 1,2-dichloroethane. This catalyst is efficient for the oxidation of cyclooctene, with a moderate 100% selectivity for epoxidation with 97% conversion in 30 min. We were able to separate the supermagnetic nanocatalyst by using an external magnetic field, and to use the catalyst at least five successive times without significant decrease in conversion. The proposed supermagnetic nanocatalyst has advantages in catalytic activity, selectivity, catalytic reaction time and reusability by easy separation.
机译:制备了一种新型的在超顺磁性纳米粒子上的辅助分支包覆的氧-过氧Mo(VI)四齿席夫碱配合物,并通过红外光谱,X射线粉末衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),振动样品磁力分析(VSM),漫反射光谱(DRS)和原子吸收光谱(AAS)。使用叔丁基过氧化氢作为氧化剂在1,2-二氯乙烷中使用该催化剂进行环辛烯,环己烯,苯乙烯,茚,α-pine烯,1-庚烯,1-辛烯,1-十二烯和反-对苯乙烯的选择性环氧化。该催化剂对环辛烯的氧化有效,在30分钟内对环氧化的选择性为100%,转化率为97%。我们能够通过使用外部磁场分离超磁性纳米催化剂,并连续至少五次使用该催化剂,而转化率却没有显着降低。所提出的超磁性纳米催化剂通过易于分离在催化活性,选择性,催化反应时间和可重复使用性方面具有优势。

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