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Green and Sustainable Tandem Catalytic Approach for Fine-Chemicals Synthesis Using Octahedral MnO2 Molecular Sieve: Catalytic Activity versus Method of Catalyst Synthesis

机译:八面体MnO2分子筛合成精细化工的绿色可持续串联催化方法:催化活性与催化剂合成方法的比较

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Octahedral MnO2 molecular sieve (OMS) was prepared using a hydrothermal synthesis route in the absence and the presence of urea. OMS was also prepared by a solvent-free method. Catalysts were characterized by the complementary combination of X-ray diffraction, N2 adsorption, scanning electron microscopy, UV-visible spectroscopy, thermogravimetric analysis, and NH3 and CO2 temperature-programmed desorption techniques. Catalysts were investigated in the oxidation of benzyl alcohols, hydration of aromatic/heterocyclic nitrile, and condensation reactions (Knoevenagel and Aldol). Furthermore, applicability of the catalyst was extended in one-pot tandem conversion of benzyl alcohol to 2-benzylidene-malononitrile, (E)-chalcone, and 2,3-dihydro-1,5-benzothiaze-pine. 2-Benzylidene-malononitrile and (E)-chalcone were prepared by a two-step tandem reaction from benzyl alcohol, whereas 2,3-dihydro-1,5-benzothiazepine was prepared by a three-step tandem reaction from benzyl alcohol. Recycling study showed that no significant decrease in the catalytic activity was observed even after five recycles. To the best of our knowledge, this is the first report that shows that OMS materials obtained using different synthesis methods exhibited significant differences in their catalytic activity in the above-mentioned reactions.
机译:在不存在和存在尿素的情况下,使用水热合成路线制备了八面体MnO2分子筛(OMS)。 OMS也通过无溶剂方法制备。催化剂的特征是通过X射线衍射,N2吸附,扫描电子显微镜,紫外可见光谱,热重分析以及NH3和CO2程序升温脱附技术的互补组合来表征的。在苯甲醇的氧化,芳族/杂环腈的水合以及缩合反应(Knoevenagel和Aldol)中研究了催化剂。此外,该催化剂的适用性扩展为将苄醇一锅串联转化为2-亚苄基-丙二腈,(E)-查耳酮和2,3-二氢-1,5-苯并噻嗪-松。通过苄基醇的两步串联反应制备2-苄基-丙二腈和(E)-查尔酮,而通过苄基醇的三步串联反应制备2,3-二氢-1,5-苯并噻氮平。回收研究表明,即使经过五次回收,催化活性也没有明显降低。据我们所知,这是第一份报告,表明使用不同合成方法获得的OMS材料在上述反应中的催化活性表现出显着差异。

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