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Nitro group reduction and Suzuki reaction catalysed by palladium supported on magnetic nanoparticles modified with carbon quantum dots generated from glycerol and urea

机译:负载在甘油和尿素生成的碳量子点修饰的磁性纳米粒子上的钯催化的硝基还原和铃木反应

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摘要

Glycerol and urea were used as green and cheap sources of carbon quantum dots (CQD) for modifying Fe3O4 nanoparticles (NPs). The obtained CQD@Fe3O4 NPs were used for the stabilization of palladium species and the prepared catalyst, Pd@CQD@Fe3O4, was characterized using various techniques. This magnetic supported palladium was applied as an efficient catalyst for the reduction of aromatic nitro compounds to primary amines at room temperature using very low palladium loading (0.008 mol%) and also for the Suzuki–Miyaura cross-coupling reaction of aryl halides as well as challenging heteroaryl bromides and aryl diazonium salts with arylboronic acids and with potassium phenyltrifluoroborate. This magnetically recyclable catalyst was recovered and reused for seven consecutive runs in the reduction of 4-nitrotoluene to p-toluidine and for ten consecutive runs in the reaction of 4-iodoanisole with phenylboronic acid with small decrease of activity. The catalyst reused in the Suzuki reaction was characterized using transmission electron microscopy, vibrating sample magnetometry and X-ray photoelectron spectroscopy. Using experiments such as hot filtration and poisoning tests, it has been shown that the true catalyst works under homogeneous conditions according to the release–return pathway of active palladium species.
机译:甘油和尿素被用作绿色廉价的碳量子点(CQD)来源,用于修饰Fe3O4纳米粒子(NPs)。将获得的CQD @ Fe3O4 NP用于稳定钯物种,并使用多种技术对制得的催化剂Pd @ CQD @ Fe3O4进行了表征。这种磁性负载的钯被用作有效的催化剂,用于在室温下使用非常低的钯负载量(0.008 mol%)将芳族硝基化合物还原为伯胺,还用于芳烃卤化物的Suzuki-Miyaura交叉偶联反应以及具有挑战性的杂芳基溴化物和芳基重氮盐与芳基硼酸和苯基三氟硼酸钾。回收该可磁循环的催化剂,并在4-硝基甲苯还原为对甲苯胺的过程中连续使用七次,并在4-碘苯甲醚与苯基硼酸的反应中连续十次重复使用,但活性降低很小。使用透射电子显微镜,振动样品磁法和X射线光电子能谱对在Suzuki反应中重复使用的催化剂进行了表征。使用热过滤和中毒试验等实验,已经证明,根据活性钯物质的释放-返回途径,真正的催化剂可以在均相条件下工作。

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