Synthesis, characterization, and cytotoxicity studies of diimine derivatives and their ruthenium(II)-p-cymene complexes

被引:0
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作者
Davila-Silva, Alicia [1 ]
Martínez-Estévez, Mónica [1 ,2 ]
Lorenzo, Aida [1 ,2 ]
García-Fontán, Soledad [1 ,2 ]
Vázquez-López, Ezequiel M. [1 ,2 ]
机构
[1] Departamento de Química Inorgánica, Campus Universitario, Universidade de Vigo, Vigo,E-36310, Spain
[2] Metallosupramolecular Chemistry Group, Galicia South Health Research Institute (IIS Galicia Sur) SERGAS-UVIGO, Vigo,E-36213, Spain
关键词
Chlorine compounds - Condensation reactions - Cytotoxicity - Ruthenium compounds - Spectroscopic analysis - Synthesis (chemical);
D O I
10.1016/j.poly.2024.117269
中图分类号
学科分类号
摘要
The reaction of five di-imines obtained by condensation of etilendiamine with 4-hydroxybenzaldehyde (L1), 2,4-dihydroxibenzaldehyde (L2) and 1-(2,4-dihydroxyphenyl)ethan-1-one (L3) or, condensations of glyoxal with 4-aminophenol (L4) and 4-amino-3-fluorphenol (L5) with [Ru2(Cl)4(η6-p-cymene)2] was studied. In absence of silver salts, four cationic complexes of formula [RuCl(η6-p-cymene)(Ln)]X where n = 1, 3, 4 and X = Cl and, n = 5 and X = PF6 could be isolated as pure solid materials. The complexes were characterized by different spectroscopic techniques and the X-ray structures of the L1 hydrate and its complex [RuCl(η6-p-cymene)(L1)]Cl were also determined. These studies confirm the N,N’-bidentate nature of the ligand L1 and the pseudo-octahedral geometry of the ruthenium coordination environment in the complex. Furthermore, the complex derived from L3, shows a potent cytotoxic activity against tumor cell line A549. © 2024 The Author(s)
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