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The synthesis of biphenyl through C-H bond activation in benzene over a Pd catalyst supported on graphene oxide

机译:在氧化石墨烯基辛催化剂上通过C-H键活化在苯氧化物中的C-H键活化合成

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This is the first report on carbon-hydrogen (C-H) bond activation in benzene over a palladium catalyst supported on graphene oxide (GO) leading to the sole formation of biphenyl with a yield of 78%. The reaction was performed for 12 h in the presence of acetic acid and oxygen at 80 degrees C. XPS studies indicated that in the initial catalyst, Pd is mainly present as Pd(ii) species on the GO surface. The interaction of these species with acetic acid during the reaction generates Pd acetate species. Density functional theory (DFT) studies revealed that the adsorption of the first benzene molecule on the Pd acetate is weak (0.15 eV) and the energy barrier of the following C-H bond scission is high, equal to 1.67 eV. The adsorption of the second benzene molecule is relatively strong (0.40 eV); acetic acid molecules are then released, leaving the biphenyl Pd intermediate, which enables biphenyl molecule formation. The presence of oxygen and acetic acid is needed for closing the catalytic cycleviathe regeneration of the reactive Pd acetate.
机译:这是苯上碳氢(C-H)键活化的第一个报告在石墨烯氧化物(GO)上负载的钯催化剂上,导致苯苯基的唯一形成,产率为78%。在乙酸存在下进行12小时,在80℃下进行12小时,XPS研究表明,在初始催化剂中,Pd主要在去表面上作为Pd(II)物种。在反应过程中,这些物种与乙酸的相互作用产生Pd乙酸盐物质。密度函数理论(DFT)研究表明,第一个苯分子对Pd乙酸盐的吸附是弱(0.15eV),并且以下C-H键槽的能量屏障高,等于1.67eV。第二苯分子的吸附相对强(0.40eV);然后释放乙酸分子,离开联苯Pd中间体,其能够形成联苯的分子。需要氧气和乙酸的存在来关闭催化性循环脂肪酸的反应性Pd乙酸盐的再生。

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