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Synthesis, crystal and electronic structure, anticancer activity of ruthenium(ll) arene complexes with thiosemicarbazones

机译:钌(II)芳烃与硫代半氨基甲酮的合成,晶体和电子结构及抗癌活性

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摘要

A series of half-sandwich ruthenium(ll) arene complexes [(η~6-p-cymene)Ru"(R-BzTSC)CI]CI 1-3 (BzTSC = benzaldehyde thiosemicarbazone and R = H, CH3 and C6H5) have been synthesized and characterized by IR, ~1H NMR, UV-visible, electrospray ionization mass spectrometry and elemental analysis. The single-crystal structures of 1 and 3 have been determined. The molecular orbitals and electronic absorption spectra of the compounds have been calculated using the DFT and TDDFT methods. The in vitro antiproliferative activities of these complexes have been evaluated against four human cancer cell lines (CNE, H292, SKBR3 and Heyl-B), and 3 is proved to be the most efficient inhibitor, with IC_(50) values of 20, 31,10 and 34 μm, respectively.
机译:一系列半三明治钌(II)芳烃配合物[(η〜6-对-cymene)Ru“(R-BzTSC)Cl] Cl 1-3(BzTSC =苯甲醛硫代半碳酮,R = H,CH3和C6H5)通过红外光谱,〜1H NMR,紫外可见光,电喷雾电离质谱和元素分析对其进行合成和表征,确定了1和3的单晶结构,并使用该化合物计算了该化合物的分子轨道和电子吸收光谱已经评估了这些复合物对四种人类癌细胞系(CNE,H292,SKBR3和Heyl-B)的体外抗增殖活性,其中3种被证明是最有效的抑制剂,IC_(50 )值分别为20、31、10和34μm。

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