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作 者:贾士芳[1] 郝秀丽 温艳珍[1] 张燕[1] JIA Shi-Fang;HAO Xiu-Li;WEN Yan-Zhen;ZHANG-Yan(School of Chemical and Biological Engineering,Taiyuan Science and Technology University,Taiyuan 030021,China)
机构地区:[1]太原科技大学化学与生物工程学院,太原030021
出 处:《无机化学学报》2022年第10期1919-1926,共8页Chinese Journal of Inorganic Chemistry
基 金:山西省高等学校科技创新项目(No.2020L0334)资助。
摘 要:设计并合成了3个含有席夫碱基团的配体(BL^(n),n=1~3)及相应的双核联吡啶钌配合物[Ru(BL^(n))(bpy)_(2)]_(2)(ClO_(4))_(4),其中bpy=2,2'⁃联吡啶,BL^(n)=((PyCHN)⁃Ph⁃O⁃C_(6)H_(4))_(2)R(PyCHN=N⁃2⁃吡啶亚甲基,R=none(Ru1),—C(CH_(3))_(2)(Ru2),—SO_(2)(Ru3))。通过元素分析、核磁氢谱、红外光谱、质谱等方法对配体和配合物进行了表征。通过体外细胞毒性实验研究了Ru1~Ru3对宫颈癌细胞(Hela)、胃癌细胞(BGC823)、胃癌细胞(SGC⁃7901)三种肿瘤细胞和人正常胚肺成纤维细胞MRC⁃5的细胞毒性,实验结果表明Ru3的抗肿瘤活性最好,而Ru1~Ru3均对BGC823具有选择性。A series of new Schiff base ligands(BL^(n),n=1⁃3)and complexes have been synthesized.Binuclear ruthenium complexes[Ru(BL^(n))(bpy)_(2)]_(2)(ClO_(4))_(4),where bpy=2,2'⁃bipyridine,BL^(n)=((PyCHN)⁃Ph⁃O⁃C_(6)H_(4))_(2)R(PyCHN=N⁃2⁃pyridylmethylene,R=none for Ru1,—C(CH_(3))_(2) for Ru2 and—SO_(2) for Ru3),have been prepared and character⁃ized by element analysis,1H NMR,IR,and mass spectrometry methods.The cytotoxicity to cervical cancer cells(Hela),gastric cancer cells(BGC823),gastric cancer cells(SGC⁃7901),and human normal embryonic lung fibroblasts cells(MRC⁃5)of the three complexes in vitro was evaluated using the 3⁃(4,5⁃dimethylthiazol⁃2⁃yl)⁃2,5⁃diphenyltetrazolium bromide assay.It is worth noting that Ru1⁃Ru3 showed excellent antitumor effects in a cellular study for BGC823 in vitro.However,Ru3 exhibited the highest cytotoxicity to any cancer cells than Ru1 and Ru2.
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