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首页> 外文期刊>Current Organocatalysis >Fe_3O_4@Sio2 Nanoparticles Decorated with Schiff base Complex of Pd(II) as a Magnetically Phosphine-free Catalyst for Heck-Mizoroki Coupling Reactions
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Fe_3O_4@Sio2 Nanoparticles Decorated with Schiff base Complex of Pd(II) as a Magnetically Phosphine-free Catalyst for Heck-Mizoroki Coupling Reactions

机译:Fe_3O_4 @ SiO2纳米粒子用Pd(II)的Schiff碱基综合体装饰为磁性磷酸 - Mizoroki偶联反应的催化剂

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Background: The palladium-catalyzed couplings of alkenes with aryl halides is considered as one of the most important methods for carbon-carbon bond formation and have been utilized in the areas of natural products, high performance materials, bioactive compounds, new drugs and many industrially useful chemicals. Although the homogeneous palladium catalysts offer several advantages concerning higher selectivity and yields, better tuning of chemoselectivity and high efficiency but commercializing most of homogeneous has not been possible because of recycling problem of the catalyst from the mixture of reaction. Therefore, for resolving this problem, immobilization of homogeneous Pd complexes via grafting to solid supports such as activated carbon, zeolites, silica or modified silica, polymers, nanoparticles, and magnetic core shells have been subject of great challenges. Methods: Fe_3O_4 nanoparticles was coated by silica gel and then decorated by Schiff base Pd complex to provide Fe_3O_4@SiO_2/Schiff base/Pd(II) nanoparticles. After optimization of reaction parameters, Heck-Mizoroki coupling reaction of aryl halides with olefins was studied. Results: The magnetic Schiff base complex of Pd, as a phosphine free nanocatalyst, catalyzed efficiently Heck-Mizoroki carbon-carbon coupling reaction between aryl halides and alkenes and provided the desired products in high yields. The magnetic Pd complex was easily removed from the reaction mixture and reused for eight runs. Conclusion: A new efficient, simple and cost effective protocol was introduced for carbon-carbon bond formation via Heck-Mizoroki coupling reaction of aryl halides with olefins in high to excellent yields in short reaction times. These valuable advantages were achieved because of employing Fe_3O_4@SiO_2/Schiff base/Pd(II) complex as a dispersible, phosphine free ligand, highly active, magnetically recoverable and reusable several times.
机译:背景:具有芳基卤化物烯烃的钯催化的偶联被认为是碳 - 碳键形成最重要的方法之一,并已在天然产物,高性能材料,生物活性化合物,新药和许多工业方面使用有用的化学品。虽然均相钯催化剂有关较高的选择性和产率的若干优点,但由于从反应的混合物中回收催化剂的回收问题,因此不可能更好地调整化学选择性和高效率,但商业化大多数均匀化。因此,为了解决该问题,通过移植到固体载体,例如活性炭,沸石,二氧化硅或改性二氧化硅,聚合物,纳米颗粒和磁芯壳的均匀Pd络合物的固定已经受到巨大挑战。方法:通过硅胶涂覆Fe_3O_4纳米颗粒,然后通过Schiff碱Pd络合物装饰,提供Fe_3O_4 / Schiff Base / Pd(II)纳米颗粒。在优化反应参数之后,研究了芳基卤化物与烯烃的Heck-Mizoroki偶联反应。结果:Pd的磁性席克碱基复合物,作为磷酸纳米催化剂,催化芳基卤化物和烯烃在芳基和烯烃之间的碳 - 碳偶联反应,并提供高产率的所需产物。磁性Pd络合物容易从反应混合物中除去并重复使用8个润。结论:通过Heck-Mizoroki芳基卤化物与烯烃与烯烃的偶联反应引入新的高效,简单和成本效率的方案,其在短反应时间内高于优异的产率。由于采用Fe_3O_4 / Schiff Base / Pd(II)复合物作为可分散的,磷化氢配体,高活性,磁能可回收和可重复使用,因此实现了这些有价值的优点。

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