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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis, characterisation, cytotoxicity and antibacterial activity of ruthenium(II) and rhodium(III) complexes with sulfur-containing terpyridines
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Synthesis, characterisation, cytotoxicity and antibacterial activity of ruthenium(II) and rhodium(III) complexes with sulfur-containing terpyridines

机译:钌(II)和铑(III)与含硫三联吡啶的配合物的合成,表征,细胞毒性和抗菌活性

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摘要

The synthesis and characterisation of novel thioacetyl-functionalised terpyridine ligands and their ruthenium and rhodium complexes [Ru(tpy)(2)](PF6)(2), [Rh(tpy)(2)](PF6)(3), [Ru(phen)(tpy)Cl](PF6), [Rh(phen)(tpy) Cl](PF6)(2) (phen = phenanthroline; tpy = S-[omega-(2,2:6',2 ''-terpyridin-4'-yl)phenoxy]alkyl ethanethioate) have been described. Ligands and complexes were characterised by H-1 NMR spectroscopy, mass spectrometry, elemental analysis and cyclic voltammetry data. The crystal structure of the complex [Rh (phen)(tpy)Cl](PF6)(2) (phen = phenanthroline; tpy = 4'-phenyl-2,2':6',2 ''-terpyridine) (21), have been determined by X-ray crystallography. Complex 21 show a distorted octahedral geometry around the ruthenium centre. Antimicrobial activity toward Escherichia coli at concentrations as low as 5 mu M was found for some of the studied complexes. For complexes [Rh(tpy-C6H4-O(CH2)(8)-SCOCH3)(2)](PF6)(3) (19), [Rh(phen)(tpy-C6H4-O-(CH2)(8)-SCOCH3)Cl](PF6)(2) (31) and [Rh(phen)(tpy-C6H4-O-(CH2)(11)-SCOCH3)Cl](PF6)(2) (32), a strong inhibition of in vitro protein synthesis was observed using firefly luciferase. An investigation of cytotoxicity of the complexes against human embryonic kidney cells (HEK293 line) by the MTT assay demonstrates that the toxicity of all tested compounds is of similar magnitude, with IC50 values of 3-30 mu M. (C) 2016 Elsevier Ltd. All rights reserved.
机译:新型硫代乙酰基官能化的吡啶吡啶配体及其钌和铑配合物[Ru(tpy)(2)](PF6)(2),[Rh(tpy)(2)](PF6)(3),[ Ru(phen)(tpy)Cl](PF6),[Rh(phen)(tpy)Cl](PF6)(2)(phen =菲咯啉; tpy =S-ω-(2,2:6',2已经描述了“-叔吡啶-4'-基)苯氧基]烷基乙硫醇酯。配体和配合物通过H-1 NMR光谱,质谱,元素分析和循环伏安数据进行表征。配合物[Rh(phen)(tpy)Cl](PF6)(2)的晶体结构(phen =菲咯啉; tpy = 4'-苯基-2,2':6',2''-叔吡啶)(21 ),已通过X射线晶体学测定。配合物21在钌中心周围显示出扭曲的八面体几何形状。对于某些研究的复合物,发现其对大肠杆菌的抗菌活性低至5μM。对于络合物[Rh(tpy-C6H4-O(CH2)(8)-SCOCH3)(2)](PF6)(3)(19),[Rh(phen)(tpy-C6H4-O-(CH2)(8 )-SCOCH3)Cl](PF6)(2)(31)和[Rh(phen)(tpy-C6H4-O-(CH2)(11)-SCOCH3)Cl](PF6)(2)(32),使用萤火虫荧光素酶观察到强烈抑制体外蛋白质合成。通过MTT分析研究复合物对人类胚胎肾细胞(HEK293品系)的细胞毒性,表明所有测试化合物的毒性具有相似的程度,IC50值为3-30μM。(C)2016 Elsevier Ltd.版权所有。

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