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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Palladium supported on bis(indolyl)methane functionalized magnetite nanoparticles as an efficient catalyst for copper-free Sonogashira-Hagihara reaction
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Palladium supported on bis(indolyl)methane functionalized magnetite nanoparticles as an efficient catalyst for copper-free Sonogashira-Hagihara reaction

机译:双(吲哚基)甲烷官能化磁铁矿纳米颗粒上负载的钯作为无铜Sonogashira-Hagihara反应的有效催化剂

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摘要

A novel heterogeneous catalyst based on palladium nanoparticles supported on 3,3'-bisindolyl(4-hydroxyphenyl)methane functionalized magnetite (Fe3O4) nanoparticles was synthesized, characterized and used as catalyst for Sonogashira-Hagihara reaction. The alkynylation of a variety of aryl iodides and aryl bromides with terminal alkynes was carried out at 60 degrees C under copper and phosphane-free conditions using N,N-dimethyl acetamide as solvent, DABCO as base and low Pd loadings (0.18 mol%) under air. In the case of aryl chlorides, the reaction was carried out at 120 degrees C in the presence of tetra-n-butylammonium bromide (TBAB) and 0.36 mol% of Pd catalyst. The heterogeneous palladium catalyst introduced in this study is recoverable by an external magnet and it can be used for seven consecutive runs without a significant loss in catalytic activity. (C) 2016 Elsevier B.V. All rights reserved.
机译:合成了一种新型的基于负载在3,3'-双吲哚基(4-羟苯基)甲烷官能化磁铁矿(Fe3O4)纳米颗粒上的钯纳米颗粒的非均相催化剂,表征并用作Sonogashira-Hagihara反应的催化剂。各种芳基碘化物和芳基溴化物与末端炔烃的炔基化反应是在60℃,无铜和膦的条件下,使用N,N-二甲基乙酰胺作为溶剂,DABCO作为碱和低Pd含量(0.18 mol%)进行的在空中。在芳基氯的情况下,反应在四正丁基溴化铵(TBAB)和0.36mol%的Pd催化剂的存在下在120℃下进行。在本研究中引入的多相钯催化剂可通过外部磁体回收,并且可以连续七次使用,而不会显着降低催化活性。 (C)2016 Elsevier B.V.保留所有权利。

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