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Chemoselective hydrogenation of 3-nitrostyrene over a Pt/FeOx pseudo-single-atom-catalyst in CO2-expanded liquids

机译:在CO2膨胀液体中的Pt / FeOx假单原子催化剂上对3-硝基苯乙烯进行化学选择性加氢

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摘要

Chemoselective hydrogenation of substituted nitroarenes containing two reducible groups in one molecule is a highly desired approach to the synthesis of functionalized anilines. To make this process environmentally benign, we used a pseudo-single-atom-catalyst Pt/FeOx and investigated the reaction in supercritical CO2 and CO2-expanded toluene. The results showed that supercritical CO2 afforded excellent selectivity but low reactivity due to the limited substrate solubility in the reaction medium. By contrast, when the reaction proceeded in CO2 expanded toluene, both the conversion of 3-nitrostyrene and the selectivity of 3-vinylaniline reached above 95% under optimum conditions while the organic toluene amount could be reduced by 90% compared to that without CO2. The thermodynamic calculations revealed that the solubility of H-2 increased while the viscosity of the reaction system decreased with the CO2 pressure, which facilitated the mass transfer and therefore increased the reaction rate meanwhile keeping the selectivity at a high level.
机译:在一个分子中包含两个可还原基团的取代硝基芳烃的化学选择氢化是合成功能化苯胺的高度期望的方法。为了使该过程对环境无害,我们使用了伪单原子催化剂Pt / FeOx并研究了在超临界CO2和CO2膨胀的甲苯中的反应。结果表明,由于底物在反应介质中的溶解度有限,超临界CO2具有出色的选择性,但反应性却很低。相反,当反应在CO2膨胀的甲苯中进行时,在最佳条件下,3-硝基苯乙烯的转化率和3-乙烯基苯胺的选择性均达到95%以上,而与不使用CO2的情况相比,有机甲苯的量可减少90%。热力学计算表明,H-2的溶解度随CO2压力的增加而增加,反应体系的粘度降低,这有利于传质,因此提高了反应速率,同时保持了较高的选择性。

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