首页> 外文OA文献 >Square-planar dichloro palladium complexes with trans-configurated phosphine ligands avoiding ortho-metallation: Ligand design, complex synthesis, molecular structure and catalytic potential for Suzuki cross-coupling reactions
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Square-planar dichloro palladium complexes with trans-configurated phosphine ligands avoiding ortho-metallation: Ligand design, complex synthesis, molecular structure and catalytic potential for Suzuki cross-coupling reactions

机译:具有反式-构型膦配体的方平面二氯钯配合物,避免原位金属化:配体设计,配合物合成,分子结构和Suzuki交叉偶联反应的催化潜力

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摘要

The square-planar palladium complexes trans-[PdCl (PPh-CH-2,4,6-CHMe)] () and trans-[PdCl (η-PPh-CH-2,4,6-CHMe-CH-2,4,6-CHMe-CH-PPh)] () have been synthesized from [PdCl (cod)] (cod = 1,5-cyclooctadiene) and the corresponding new phosphine or diphosphine ligands. The single-crystal X-ray structure analysis reveals for both complexes a arrangement of the two chlorine and of the two phosphorus atoms. In both cases, -metallation leading to palladacycles is not possible, since all positions in the benzylic rings of and are blocked by methyl substituents. Both complexes are found to catalyze Suzuki cross-coupling reactions of deactivated and even bulky arene substrates.
机译:方平面钯配合物反式[PdCl(PPh-CH-2,4,6-CHMe)]()和反式[PdCl(η-PPh-CH-2,4,6-CHMe-CH-2,由[PdCl(cod)](cod = 1,5-环辛二烯)和相应的新膦或二膦配体合成了4,6-CHMe-CH-PPh)]()。单晶X射线结构分析揭示了两种络合物的两个氯原子和两个磷原子的排列。在这两种情况下,导致金属缩环的金属化都是不可能的,因为α1和β1的苄基环中的所有位置都被甲基取代基所封闭。发现这两种络合物都可以催化失活的甚至是庞大的芳烃底物的Suzuki交叉偶联反应。

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