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Metal-Free H-2 Activation for Highly Selective Hydrogenation of Nitroaromatics Using Phosphorus-Doped Carbon Nanotubes

机译:使用磷掺杂的碳纳米管的无金属H-2活化,用于高精度氢化硝基甲酰胺

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摘要

We reported that phosphorus-doped carbon nanotubes (P-CNTs), showing metal-like properties, can efficiently promote metal-free hydrogenation of nitrobenzene (1a) to aniline (2a) using molecular hydrogen (H-2) as a reducing reagent under very mild conditions with a reaction temperature of only 50 degrees C. The kinetics of 1a hydrogenation over P-CNT reveals that the hydrogenation rate of 1a is a first-order dependence on the H-2 pressure and the P-CNT loading level, and a zero-order dependence on 1a concentration, demonstrating the rate-determining step of H-2 adsorption and activation over P-CNT. The activation energy of P-CNT-catalyzed 1a hydrogenation is 43 +/- 3 kJ mol(-1) with the turnover frequency around 3.60 +/- 0.12 h(-1) at 50 degrees C. In addition to 1a, the general applicability of the P-CNT-promoted metal-free hydrogenation process is further demonstrated by applying various functionalized nitroaromatics with wide industrial interest. The P-CNT shows both excellent yields and selectivities to hydrogenation with respect to reducible, labile, and strong leaving groups on the nitroaromatics molecules. The stability and reusability of the P-CNT demonstrate up to eight-time recycling without evident loss of activity and selectivity. In addition to hydrogenation, metal-free catalytic transfer hydrogenation of 1a is achieved with P-CNT using diverse hydrogen sources, including hydrazine hydrate (N2H4 center dot H2O), carbon monoxide/water (CO/H2O), and formic acid/triethylamine (HCOOH/Et3N).
机译:我们报道了磷掺杂的碳纳米管(P-CNT),显示金属样性能,可以使用分子氢(H-2)作为还原试剂有效地促进硝基苯(1A)至苯胺(2A)的无金属氢化非常温和的条件,反应温度仅为50℃。1A氢化对P-CNT的动力学表明,1A的氢化速率是对H-2压力和P-CNT负载量水平的一阶依赖性,以及对1A浓度的零阶依赖性,证明H-2吸附和激活对P-CNT的速率确定步骤。 P-CNT催化的1A氢化的活化能是43 +/- 3kJ摩尔(-1),周转频率为3.60 +/- 0.12 h(-1),在50℃下。除了1a,一般通过施加具有宽工业利益的各种官能化的硝基甲族学,进一步证明了P-CNT促进的无金属氢化过程的适用性。 P-CNT在硝基甲族分子上的可再氧化,不稳定和强的基团上表明优异的产率和选择性。 P-CNT的稳定性和可重用性在没有明显丧失活动和选择性的情况下展示了最多八次回收。除了氢化外,使用不同氢气源的P-CNT实现1A的无金属催化转移氢化,包括肼水合物(N2H4中心点H2O),一氧化碳/水(CO / H2O)和甲酸/三乙胺( HCOOH / ET3N)。

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  • 来源
    《ACS applied materials & interfaces》 |2020年第1期|共13页
  • 作者单位

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

    Jinan Univ Guangdong Engn &

    Technol Res Ctr Graphene Like Ma Dept Chem Coll Chem &

    Mat Sci 601 Huangpu Ave West Guangzhou 510632 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    carbocatalysis; kinetics; metal-free; selective hydrogenation; transfer hydrogenation;

    机译:CARBOCATALALY;动力学;无金属;选择性氢化;转移氢化;

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