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首页> 外文期刊>Catalysis Letters >Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)(6) as Carbonyl Source
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Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)(6) as Carbonyl Source

机译:生物钯络合物固定在中孔SBA-16上:使用Cr(CO)(6)作为羰基源的芳基碘化物和芳基硼酸的羰基铃木偶联反应的有效的异质催化剂

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摘要

In this study, a binuclear palladium complex immobilized on the organo-functionalized SBA-16 was prepared and structurally characterized by routine techniques. Characterizations indicated that the mesostructure of SBA-16 was maintained after the immobilization of palladium complex. Then, the prepared nanomaterial was applied as a heterogeneous catalyst in the carbonylative Suzuki coupling reaction of aryl iodides with arylboronic acids using Cr(CO)(6) as carbonyl source. The catalyst was efficiently promoted the coupling reactions of various aryl iodides and arylboronic acids to give the corresponding diaryl ketones in excellent yields. Moreover, the catalyst was readily recovered by filtration and could be reused for seven cycles without losing its structural integrity and catalytic activity. Graphic
机译:在该研究中,制备固定在有机官能化的SBA-16上的双核钯络合物并通过常规技术进行结构表征。 表征表明,在固定钯配合物的固定后,将保持SBA-16的腹部结构。 然后,使用Cr(CO)(6)作为羰基源的芳基碘化物的芳基碘化物的羰基铃木偶联反应中制备的纳米材料作为异质催化剂。 催化剂得到有效促进各种芳基碘和芳基硼酸的偶联反应,得到相应的二芳基酮以优异的产率。 此外,通过过滤容易地回收催化剂,并且可以重复使用7个循环,而不会损失其结构完整性和催化活性。 形象的

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