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Nanoporous Gold Catalyst for Highly Selective Semihydrogenation of Alkynes: Remarkable Effect of Amine Additives

机译:炔烃高度选择性半氢化的纳米孔金催化剂:胺类添加剂的显着效果

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摘要

We report for the first time the highly selective semihydrogenation of alkynes using the unsupported nanoporous gold (AuNPore) as a catalyst and organosilanes with water as a hydrogen source. Under the optimized reaction conditions, the present semihydrogenation of various terminal- and intemal- alkynes affords the corresponding alkenes in high chemical yields and excellent Z-selectivity without any over-reduced alkanes. The use of DMF as solvent, which generates amines in situ, or pyridine as an additive is crucial to suppress the association of hydrogen atoms on AuNPore to form H_2 gas, which is unable to reduce alkynes on the unsupported gold catalysts. The AuNPore catalyst can be readily recovered and reused without any loss of catalytic activity. In addition, the SEM and TEM characterization of nanoporosity show that the AuNPore catalyst has a bicontinuous 3D structure and a high density of atomic steps and kinks on ligament surfaces, which should be one of the important origins of catalytic activity.
机译:我们首次报道了使用无载体的纳米孔金(AuNPore)作为催化剂和有机硅烷以水为氢源对炔烃进行高度选择性的半氢化反应。在优化的反应条件下,目前各种末端和中间炔烃的半氢化反应可在高化学收率和出色的Z选择性的情况下提供相应的烯烃,而不会出现烷烃过度还原的情况。使用DMF作为溶剂可在原位生成胺,或使用吡啶作为添加剂,对于抑制AuNPore上的氢原子缔合形成H_2气体至关重要,这无法还原未负载金催化剂上的炔烃。 AuNPore催化剂可以容易地回收和再利用而没有任何催化活性的损失。另外,SEM和TEM表征的纳米孔隙度表明AuNPore催化剂具有双连续的3D结构和在韧带表面的高密度的原子台阶和纽结,这应该是催化活性的重要来源之一。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第42期|17536-17542|共7页
  • 作者单位

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    Institute for International Advanced Interdisciplinary Research (IIAIR), International Advanced Research and Education Organization, Tohoku University, Sendai, 980-8578, Japan,Taketoshi Minato, Office of Society-Academia Collaboration for Innovation, Kyoto University Gokasho, Uji, Kyoto 611- 0011, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012, China;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan;

    WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan,State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012, China;

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