首页> 外文期刊>Journal of Molecular Liquids >Hydrophilic role of deep eutectic solvents for clean synthesis of biphenyls over a magnetically separable Pd-catalyzed Suzuki-Miyaura coupling reaction
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Hydrophilic role of deep eutectic solvents for clean synthesis of biphenyls over a magnetically separable Pd-catalyzed Suzuki-Miyaura coupling reaction

机译:深度共晶溶剂对磁性可分离的PD催化铃木瘤偶联反应清洁合成双共晶溶剂的亲水性作用

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The development of an efficient and sustainable catalytic system for the preparation of biphenyls through the Suzuki-Miyaura coupling reaction is still a great challenge to green chemistry. Encouraging the prevailing challenge, in the present work, a heterogeneous Pd catalyst was synthesized through a green method and used for the production of biphenyls in deep eutectic solvents (DESs) as green reaction media. In order to prepare the catalyst, magnetite-graphene oxide nanocomposite was modified with cellulose via the click reaction and applied as support for Pd nanoparticles. Cellulose acted as both reducing and stabilizing agent for Pd nanoparticles and eliminated the requirement of a reducing agent. The prepared catalyst was characterized by different methods such as FT-IR, EDX, EDX-mapping, XPS, SEM, TEM, XRD, VSM, and ICP-OES analyses. Catalytic properties of the obtained catalyst was explored in the coupling reaction of aryl halides with aryl boronic acids in different hydrophilic and hydrophobic DESs. The presence of cellulose with hydrophilic character on the structure of catalyst offered well dispersion of the catalyst in hydrophilic DESs, which led to enhancement of its catalytic activity. Among various hydrophilic DESs, the DES composed of dimethylammonium chloride and glycerol was verified as the most effective solvent for the preparation of biphenyls. The catalyst was compatible with a variety of substrates, with which all the Suzuki coupling products were achieved in high to excellent yields. Thanks to the low solubility of catalyst and DES in organic solvents, the separated aqueous phase containing both of the catalyst and DES could be readily recovered by evaporating water and reused up to five successive runs with a stable activity. This simple and new separation strategy provided a clean and highly efficient synthetic methodology for the synthesis of various biphenyls. Moreover, hot filtration test efficiently confirmed that the catalyst is heterogeneous and completely stable under reaction conditions. (C) 2020 Elsevier B.V. All rights reserved.
机译:开发高效、可持续的催化体系,通过铃木-宫村偶联反应制备联苯,仍然是绿色化学的一大挑战。鼓励当前的挑战,在本工作中,通过绿色方法合成了一种多相钯催化剂,并将其作为绿色反应介质用于在深共晶溶剂(DES)中生产联苯。为了制备催化剂,通过点击反应用纤维素对磁铁矿-石墨烯氧化物纳米复合材料进行改性,并将其用作钯纳米颗粒的载体。纤维素作为钯纳米颗粒的还原剂和稳定剂,消除了对还原剂的要求。采用FT-IR、EDX、EDX图谱、XPS、SEM、TEM、XRD、VSM和ICP-OES分析等方法对制备的催化剂进行了表征。在不同的亲水性和疏水性des中,考察了所得催化剂在芳基卤化物与芳基硼酸偶联反应中的催化性能。催化剂结构上具有亲水性的纤维素的存在使催化剂在亲水性des中分散良好,从而提高了其催化活性。在各种亲水性DES中,由二甲基氯化铵和甘油组成的DES被证实是制备联苯最有效的溶剂。该催化剂与多种基质相容,所有铃木偶联产物均以高到优异的产率获得。由于催化剂和DES在有机溶剂中的溶解度较低,分离出的同时含有催化剂和DES的水相可以通过蒸发水很容易地回收,并以稳定的活性重复使用多达五次。这种简单而新的分离策略为各种联苯的合成提供了一种清洁高效的合成方法。此外,热过滤试验有效地证实了催化剂在反应条件下是非均相且完全稳定的。(C) 2020爱思唯尔B.V.版权所有。

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