首页> 外文期刊>Beilstein journal of organic chemistry. >Studies on Pd/NiFe2O4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls
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Studies on Pd/NiFe2O4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls

机译:水相中Pd / NiFe2O4催化的无配体Suzuki反应的研究:联芳基,三联苯和聚芳基的合成

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Palladium supported on nickel ferrite (Pd/NiF2O4) was found to be a highly active catalyst for the Suzuki coupling reaction between various aryl halides and arylboronic acids. The reaction gave excellent yields (70–98%) under ligand free conditions in a 1:1 DMF/H2O solvent mixture, in short reaction times (10–60 min). The catalyst could be recovered easily by applying an external magnetic field. The polyaryls were similarly synthesized.
机译:发现负载在铁氧体镍上的钯(Pd / NiF2O4)是各种芳基卤化物和芳基硼​​酸之间的Suzuki偶联反应的高活性催化剂。在无配体的条件下,在1:1 DMF / H2O溶剂混合物中,该反应在短时间内(10-60分钟)即可获得出色的收率(70-98%)。通过施加外部磁场可以容易地回收催化剂。聚芳基类似地合成。

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