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Hydrogenation of nitriles to primary amines catalyzed by an unsupported nanoporous palladium catalyst: understanding the essential reason for the high activity and selectivity of the catalyst

机译:腈的加氢主要胺由一个不受支持的纳米多孔钯催化的催化剂:了解必要的原因高的催化剂的活性和选择性

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摘要

An efficient and highly selective heterogeneous catalyst system for nitrile hydrogenation was developed using unsupported palladium nanopores (PdNPore). The PdNPore-catalyzed selective hydrogenation of nitriles proceeded smoothly, without any additives, under mild conditions (low H2 pressure and low temperature) to yield primary amines with satisfactory to excellent yields. Systematic studies demonstrated that the high activity and excellent selectivity of the PdNPore originated from its good Lewis acidity and porous structure. No palladium leached from the PdNPore during the hydrogenation reaction. Moreover, the catalyst was easily recovered and reused without any loss of catalytic activity. A deuterium-hydrogen exchange reaction clearly indicated that the present hydrogenation involves heterolytic H2 splitting on the surface of the PdNPore catalyst.
机译:一个高效和高选择性异构腈加氢催化剂体系使用不受支持的开发钯纳米孔(PdNPore)。腈的加氢进展顺利,没有任何添加剂,在温和的条件下(低H2和低温)收益率主要压力胺与满意的优秀的收益率。系统的研究表明,高PdNPore的活动和良好的选择性源于其良好路易斯酸度和多孔结构。在加氢反应。催化剂容易回收和重用催化活性的任何损失。deuterium-hydrogen交换反应明显表示,目前加氢涉及异种溶解的H2分裂表面的PdNPore催化剂。

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