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Nanosilica-anchored Pd(II)-Schiff base complex as efficient heterogeneous catalyst for activation of aryl halides in Suzuki-Miyaura cross-coupling reaction in water

机译:纳米硅基锚定Pd(II) - 作为活化芳基卤化物在水中铃木卤化物激活的高效异质催化剂

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摘要

A nanosilica (derived from rice husk)-anchored Pd(II)-Schiff base complex has been synthesized and characterized. This immobilized complex has been found to be a very effective and recyclable heterogeneous catalyst for the Suzuki-Miyaura cross-coupling reaction of various aryl halides with arylboronic acid in aqueous medium under mild conditions. The products were identified using H-1 NMR and mass spectral studies. This complex can be easily filtered out from the reaction medium and reused up to six times without significant loss of catalytic activity. Since the reaction proceeds under mild conditions in aqueous medium as well as the catalyst being recyclable, it provides an environmentally benign alternative route to the existing protocols for the Suzuki-Miyaura reaction.
机译:已经合成并表征了纳米菌(衍生自稻壳)-Schiff碱基综合体。 已经发现该固定化合物是在温和条件下,在水性培养基中具有芳基卤化物的各种芳基卤化物的Suzuki-miyaura交叉偶联反应非常有效和可回收的非均相催化剂。 使用H-1 NMR和质谱研究鉴定产物。 可以从反应介质容易地滤除该络合物,并重复使用至多六次,而不会显着损失催化活性。 由于反应在水性介质中的温和条件下进行,并且催化剂是可回收的,因此它为铃木 - 宫瓜龙反应的现有方案提供了环境良性的替代途径。

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