首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Tricyclohexylphosphine-cyclopalladated ferrocenylimine complexes: synthesis, crystal structures and application in Suzuki and Heck reactions
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Tricyclohexylphosphine-cyclopalladated ferrocenylimine complexes: synthesis, crystal structures and application in Suzuki and Heck reactions

机译:三环己基膦-环钯的二茂铁基亚胺配合物:合成,晶体结构及其在Suzuki和Heck反应中的应用

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摘要

A series of novel tricyclohexylphosphine (PCy3)-cyclopalladated ferrocenylimine complexes 2c - 2g have been easily synthesized. These new palladacycles are thermally stable and are not sensitive to air and moisture. Their detailed structures have been determined by single-crystal X-ray analysis and six different types of intermolecular hydrogen bonds are found to be existed in the crystals of these complexes. The use of 2c - 2g as catalysts for Suzuki and Heck reactions was examined. They were found to be very efficient for the Suzuki reaction of aryl chlorides with phenylboronic acid. Typically, using 0.1 mol% of catalyst in the presence of 1.5 equivalent of Cs2CO3 as base in dioxane at 100 degrees C provided coupled products in excellent yields. These complexes also displayed good activity in the Heck reaction of a range of aryl bromides with acrylic acid ethyl ester although they were not particularly useful for the activation of aryl chlorides.
机译:容易合成出一系列新型的三环己基膦(PCy3)-环钯的二茂铁亚胺配合物2c-2g。这些新的palladacycles具有热稳定性,并且对空气和湿气不敏感。它们的详细结构已通过单晶X射线分析确定,并且发现在这些配合物的晶体中存在六种不同类型的分子间氢键。考察了使用2c-2g作为Suzuki和Heck反应的催化剂。发现它们对于芳基氯与苯基硼酸的Suzuki反应非常有效。典型地,在100℃下在二恶烷中在1.5当量的Cs 2 CO 3作为碱的存在下使用0.1mol%的催化剂以优异的产率提供了偶联产物。这些配合物在一定范围的芳基溴化物与丙烯酸乙酯的Heck反应中也显示出良好的活性,尽管它们对于芳基氯化物的活化不是特别有用。

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