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Synthesis Structure of Nitrogen-ContainingPhosphinogold(I) Ferrocenes. In vitro Activity against Bladder andColon Carcinoma Cell Lines

机译:含氮化合物的合成结构磷金(I)二茂铁。抗膀胱和膀胱的体外活性结肠癌细胞系

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摘要

The gold salt [(tht)AuCl] was reacted with [1-N,N-dimethylaminométhyl-2-diphenylphosphino]ferrocene (1) forming the bimetallic derivative 4. The reaction of methyl iodide and tetramethylammonium bromide on the chloride 4 produced the ammonium salt 5 and the bromide 6 respectively. New aminophosphines 2 and 3, which represent two of the rare phosphorylated metallocenes containing P(III)-N bond have also been coordinated to gold(I) to form 7 and 8. The presence of the ethoxy group in 7 provides evidence for the lability of one nitrogen-phosphorus bond. The X-ray structure of compounds 4 and 7 have been established. Both crystallize in space group P21/c, monoclinic, with a = 11.095(2) Å, b = 12.030(3) Å, c = 17.763(4) Å, β= 94.02(2)∘, Z = 4 for 4 and a = 14.863(3) Å, b = 8.036(5)Å, c = 18.062(5)Å, β =101.64(1)°, Z = 4 for 7. 197Au Mössbauer data are in good agreement with those for other linear P-Au-Cl containing complexes. The compounds were evaluated for in vitro anti-tumour activity against two human tumours. Differential cytotoxicity was observed with activity comparable to cisplatin, with the exception of one compound which was significantly more cytotoxic.
机译:使金盐[(tht)AuCl]与[1-N,N-二甲基氨基甲基-2-二苯基膦基]二茂铁(1)反应,形成双金属衍生物4。甲基碘和溴化四甲基铵在氯化物4上的反应产生了铵盐。盐5和溴化物6。代表两个罕见的含P(III)-N键的磷酸化金属茂的新氨基膦2和3也与金(I)配位形成7和8。7中的乙氧基的存在为不稳定性提供了证据一个氮-磷键。已经建立了化合物4和7的X射线结构。两者均在空间群P21 / c中单晶结晶,a = 11.095(2)Å,b = 12.030(3)Å,c = 17.763(4)Å,β= 94.02(2)∘,Z = 4表示4和a = 14.863(3)Å,b = 8.036(5)Å,c = 18.062(5)Å,β= 101.64(1)°,Z = 4(对于7)。 197 AuMössbauer数据为与其他线性P-Au-Cl配合物的化合物具有很好的一致性。评价了化合物对两种人类肿瘤的体外抗肿瘤活性。观察到具有与顺铂相当的活性的差异性细胞毒性,除了一种具有明显更高的细胞毒性的化合物。

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