首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Benzenedicarbonyl and benzenetricarbonyl linker pyrazolyl complexes of palladium(II):synthesis,X-ray structures and evaluation as ethylene polymerisation catalysts
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Benzenedicarbonyl and benzenetricarbonyl linker pyrazolyl complexes of palladium(II):synthesis,X-ray structures and evaluation as ethylene polymerisation catalysts

机译:钯(II)的苯二羰基和苯三羰基连接基吡唑基配合物:合成,X射线结构及作为乙烯聚合催化剂的评价

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摘要

A series of novel compounds with pyrazolyl rings(pz)linked by benzenedicarbonyl(L1-L4)and benzenelricarbonyl(L5,L6)have been prepared and structurally characterized.The mutual orientation of their rings was studied by molecular mechanics.These polydentate-species react with PdCl_2(NCMe)_2 to yield dinuclear complexes in which the Pd centers coordinate to one or two pz units,a terminal chloride and two bridging chloride ligands.In complex [{(3,5-~tBu_2pzCO)_3-l ,3,5-C_6H_4}Pd_2Cl_2(mu-Cl)_2]_4 the pyrazolyl ligand L5 acts as a bidentate donor despite the presence of the third pz group.These Pd complexes,when activated with methylaluminoxidc(MAO),exhibit activity in ethylene polymerization.
机译:制备了一系列由苯二羰基(L1-L4)和苯并羰基(L5,L6)连接的吡唑基环(pz)的新型化合物并对其结构进行了表征,并通过分子力学研究了它们的环的相互取向。与PdCl_2(NCMe)_2生成双核络合物,其中Pd中心与一个或两个pz单元,一个末端氯化物和两个桥接氯化物配体配位。在络合物[{(3,5-〜tBu_2pzCO)_3-1,3, 5-C_6H_4} Pd_2Cl_2(mu-Cl)_2] _4的吡唑基配体L5尽管存在第三个pz基团,但仍充当双齿供体。这些Pd配合物在被甲基铝氧化酸(MAO)活化后在乙烯聚合中表现出活性。

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