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Ceria-supported ruthenium catalysts for the synthesis of indole via dehydrogenative N-heterocyclization

机译:二氧化铈负载的钌催化剂,用于通过脱氢N-杂环合成吲哚

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摘要

Simple heterogeneous Ru/CeO2 catalysts as well as Ru/ZrO2 catalysts were found to be quite effective for the selective direct synthesis of indole via intramolecular dehydrogenative N-heterocyclization of 2-(2-aminophenyl)ethanol, while catalysts supported on SiO2, Al2O3, TiO2, and MgO were less effective. Ru/CeO2 catalysts that were calcined at a relatively low temperature, 200 °C, showed excellent activity and gave indole in a yield over 99% by the reaction at 140 °C for 24 h (Ru catalyst 2.5 mol%). Spectroscopic studies of the Ru/CeO2 catalysts indicated the formation of Ru[IV]=O species on the surface, which is considered to be transformed into the catalytically-active species at the initial stage of the reaction. Hot filtration tests and an ICP-AES analysis indicated that these Ru/CeO2 catalysts act heterogeneously and that the leaching of ruthenium species into the solution is negligible. These catalysts could be recycled without a significant loss of activity, which suggests that the present oxide-supported catalysts are promising alternatives to conventional homogeneous catalysts.
机译:发现简单的多相Ru / CeO2催化剂以及Ru / ZrO2催化剂对于通过2-(2-氨基苯基)乙醇的分子内脱氢N-杂环化选择性地直接合成吲哚非常有效,而催化剂则负载在SiO2,Al2O3, TiO2和MgO效果较差。在相对较低的温度200°C下煅烧的Ru / CeO2催化剂显示出出色的活性,并通过在140°C下反应24小时(Ru催化剂2.5 mol%),吲哚的收率超过99%。 Ru / CeO2催化剂的光谱研究表明,Ru [IV] = O物质在表面上形成,被认为在反应的初始阶段转化为催化活性物质。热过滤测试和ICP-AES分析表明,这些Ru / CeO2催化剂的行为不均一,并且钌物种向溶液中的浸出可以忽略不计。这些催化剂可以循环使用而没有明显的活性损失,这表明本氧化物负载的催化剂是常规均相催化剂的有前途的替代品。

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