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Remarkable effect of alkalis on the chemoselective hydrogenation of functionalized nitroarenes over high-loading Pt/FeOx catalysts

机译:碱对高负载Pt / FeOx催化剂上官能化硝基芳烃化学选择性加氢的显着影响

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摘要

The chemoselective hydrogenation of substituted nitroarenes to form the corresponding functionalized anilines is an important type of reaction in fine chemistry, and the chemoselectivity is critically dependent on the rational design of the catalysts. This reaction has rarely been accomplished over high-loading Pt catalysts due to the formation of Pt crystals. Here, for the first time, we report that alkali metals (Li+, Na+, K+, etc.) can transform the non-selective high loading Pt/FeOx catalyst to a highly chemoselective one. The best result was obtained over a 5% Na–2.16% Pt/FeOx catalyst, which enhanced the chemoselectivity from 66.4% to 97.4% while the activity remained almost unchanged for the probe reaction of 3-nitrostyrene hydrogenation to 3-aminostyrene. Using aberration-corrected HAADF-STEM, in situ XAS, 57 and Fe Mössbauer and DRIFT spectroscopy, the active site of a Pt–O–Na–O–Fe-like species was proposed, which ensures that the Pt centers are isolated and positively charged for the preferential adsorption of the –NO2 group.
机译:取代的硝基芳烃的化学选择加氢反应以形成相应的官能化苯胺是精细化学中的重要反应类型,化学选择性主要取决于催化剂的合理设计。由于Pt晶体的形成,该反应很少在高负载的Pt催化剂上完成。在这里,我们首次报道碱金属(Li + ,Na + ,K + 等)可以转化非金属元素。选择性的高负载Pt / FeOx催化剂转变为高度化学选择性的催化剂。在5%Na–2.16%Pt / FeOx催化剂上可获得最佳结果,这将化学选择性从66.4%提高到97.4%,而对于3-硝基苯乙烯加氢反应生成3-氨基苯乙烯的活性几乎保持不变。使用像差校正的HAADF-STEM,原位XAS, 57 和FeMössbauer以及DRIFT光谱,提出了Pt–O–Na–O–Fe类物质的活性位点,从而确保了Pt中心被隔离并带正电荷,以优先吸附–NO2基团。

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