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TEMPO functionalized C60 fullerene deposited on gold surface for catalytic oxidation of selected alcohols

机译:TEMPO官能化的C60富勒烯沉积在金表面用于催化氧化某些醇

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摘要

C60TEMPO10 catalytic system linked to a microspherical gold support through a covalent S-Au bond was developed. The C60TEMPO10@Au composite catalyst had a particle size of 0.5–0.8 μm and was covered with the fullerenes derivative of 2.3 nm diameter bearing ten nitroxyl groups; the organic film showed up to 50 nm thickness. The catalytic composite allowed for the oxidation under mild conditions of various primary and secondary alcohols to the corresponding aldehyde and ketone analogues with efficiencies as high as 79–98%, thus giving values typical for homogeneous catalysis, while retaining at the same time all the advantages of heterogeneous catalysis, e.g., easy separation by filtration from the reaction mixture. The catalytic activity of the resulting system was studied by means of high pressure liquid chromatography. A redox mechanism was proposed for the process. In the catalytic cycle of the oxidation process, the TEMPO moiety was continuously regenerated in situ with an applied primary oxidant, for example, O2/Fe3+ system. The new intermediate composite components and the final catalyst were characterized by various spectroscopic methods and thermogravimetry. >Graphical abstract
机译:开发了通过共价S-Au键与微球金载体连接的C60TEMPO10催化系统。 C60TEMPO10 @ Au复合催化剂的粒径为0.5–0.8μm,被直径为2.3nm的富勒烯衍生物覆盖,带有10个硝氧基。有机膜的厚度可达50纳米。催化复合物可在温和条件下将各种伯醇和仲醇氧化为相应的醛和酮类似物,效率高达79–98%,因此提供了均相催化的典型值,同时保留了所有优势非均相催化的反应,例如易于通过过滤从反应混合物中分离。借助于高压液相色谱法研究了所得系统的催化活性。为该过程提出了一种氧化还原机制。在氧化过程的催化循环中,TEMPO部分用一种主要的氧化剂,例如O2 / Fe 3 + 系统连续进行原位再生。通过各种光谱学方法和热重分析法对新的中间复合材料组分和最终催化剂进行了表征。 <!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> >图形摘要<!- fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->ᅟ

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