首页> 外文期刊>Inorganica Chimica Acta >Anchoring of palladium(II) in chemically modified mesoporous silica: An efficient heterogeneous catalyst for Suzuki cross-coupling reaction
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Anchoring of palladium(II) in chemically modified mesoporous silica: An efficient heterogeneous catalyst for Suzuki cross-coupling reaction

机译:化学改性的介孔二氧化硅中钯(II)的锚固:铃木交叉偶联反应的高效多相催化剂

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摘要

The synthesis and characterization of a highly efficient and reusable catalyst, Pd(II) immobilized in mesoporous silica MCM-41, are described. Pd(II) Schiff-base moiety has been anchored onto mesoporous silica surface via silicon alkoxide chemistry. The catalyst has been characterized by small-angle X-ray diffraction (SAX), FTIR and electronic spectroscopy as well as elemental analysis. The catalyst is used in Suzuki cross-coupling reaction of various aryl halides, including less reactive chlorobenzene, and phenylboronic acid to give biaryls in excellent yields without any additive or ligand. High selectivity for the bi-aryl products containing both electron-donating and electron-withdrawing substituents, mild reaction conditions and possibility of easy recycle makes the catalyst highly desirable to address the industrial needs and environmental concerns.
机译:描述了固定在介孔二氧化硅MCM-41中的高效可重复使用的催化剂Pd(II)的合成和表征。 Pd(II)Schiff碱部分已通过硅醇盐化学方法固定在介孔二氧化硅表面上。该催化剂的特征在于小角X射线衍射(SAX),FTIR和电子光谱以及元素分析。该催化剂可用于各种芳基卤化物(包括反应性较低的氯苯)和苯基硼酸的Suzuki交叉偶联反应,以优异的收率得到联芳基,而无需任何添加剂或配体。对于同时包含给电子和吸电子取代基的联芳基产品具有高选择性,温和的反应条件以及易于回收的可能性,使得该催化剂非常需要满足工业需求和环境问题。

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