首页> 外文期刊>Inorganica Chimica Acta >Orthometallated versus coordination compounds for reactions of platinum(II) and palladium(II) with the ligand benzil bis(4-methyl-3-thiosemicarbazone)
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Orthometallated versus coordination compounds for reactions of platinum(II) and palladium(II) with the ligand benzil bis(4-methyl-3-thiosemicarbazone)

机译:用于铂(II)和钯(II)与配体苯并双(4-甲基-3-硫代半碳酰胺)反应的正金属化与配位化合物

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摘要

The ligand benzil bis(4-methyl-3-thiosemicarbazone)LH2 reacts with K2PtCl4, both in the presence or in the absence of LiOH center dot H2O, to yield simultaneously the cyclometallated mesocate [Pt-2(mu-L)(2)]1 and the coordination monomeric compound [PtL]2, which can be easily separated by their different solubility. By contrast, reaction of Li2PdCl4 without base leads exclusively to the formation of the coordination compound [PdL] 3, while the use of LiOH center dot H2O permits the selective synthesis of the cyclometallated mesocate [Pd-2(mu-L)(2)]4. All the complexes have been characterized by the usual techniques, including X-ray single crystal diffraction that show all the metals to be four-coordinate in a square-planar arrangement, but 2 and 3 with a N2S2 environment while in 1 and 4 it is CNS2. The cytotoxic activity has been evaluated against the human lung carcinoma cell line NCI-H460, but the results show that the complexes are not active in this cell line.
机译:在存在或不存在LiOH中心点H2O的情况下,配体苄基双(4-甲基-3-硫代半碳酰胺)LH2与K2PtCl4反应,同时生成环金属化的甲磺酸盐[Pt-2(mu-L)(2) ] 1和配位单体化合物[PtL] 2,它们可以通过不同的溶解度轻松分离。相比之下,没有碱的Li2PdCl4反应仅导致配位化合物[PdL] 3的形成,而使用LiOH中心点H2O则可以选择性合成环金属化的甲磺酸盐[Pd-2(mu-L)(2) ] 4。所有配合物均已通过常规技术进行了表征,包括X射线单晶衍射,显示所有金属在四平面布置中均为四配位,而2和3在N2S2环境中则在1和4中为CNS2。已经评估了针对人肺癌细胞系NCI-H460的细胞毒活性,但结果表明该复合物在该细胞系中没有活性。

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