Synthesis, crystal structure and cytotoxicity assays of a copper(II) nitrate complex with a tridentate ONO acylhydrazone ligand. Spectroscopic and theoretical studies of the complex and its ligand
| Autor: | Y. Burgos-Lopez, Reinaldo Pis-Diez, Beatriz S. Parajón-Costa, Gustavo A. Echeverría, J. Del Plá, Oscar E. Piro, Javier García-Tojal, Ana C. González-Baró, Lucia M. Balsa, Ignacio E. León |
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| Jazyk: | angličtina |
| Rok vydání: | 2019 |
| Předmět: |
Cu(II)-complex
chemistry.chemical_element Crystal structure Triclinic crystal system 010402 general chemistry DFT calculations 01 natural sciences Anticancer activity law.invention Ion Inorganic Chemistry chemistry.chemical_compound law Materials Chemistry Molecule Physical and Theoretical Chemistry Electron paramagnetic resonance Spectroscopy 010405 organic chemistry Hydrazones Chemistry Inorganic Copper Square pyramidal molecular geometry Química inorgánica 0104 chemical sciences Crystallography chemistry Copper(II) nitrate |
| Zdroj: | Repositorio Institucional de la Universidad de Burgos (RIUBU) instname |
| Popis: | The new copper complex, [Cu(HL)(OH2)2](NO3), including the tridentate N-acyhydrazone derived from 4-hydroxy-benzohydrazide and 2-hydroxy-3-methoxybenzaldehyde, (H2L), has been synthesized and characterized in the solid state and in solution by spectroscopic (FTIR, Ra, UV–vis, EPR) methods. The results were compared with those obtained for the hydrazone ligand and complemented with computational methods based on DFT. The crystal structure of the complex has been determined by X-ray diffraction. It crystallizes in the triclinic space group with Z = 2. The Cu(II) ion is in a distorted square pyramidal environment, coordinated to a planar HL- anion acting as a tridentate ligand. The 5-fold coordination is completed with two water molecules. It is arranged in the lattice as H-bonded ribbon-like polymers that extends along the [1 2 1] crystal direction. The cytotoxicity of the complex together with that of the H2L ligand and the copper ion were evaluated in vitro against five different human cancer cell lines namely A549 (lung), MG-63 (bone), MCF-7 and MDA-MB-231 (breast) and Jurkat (leukemia). The copper complex inhibits the cell viability in a dose dependent manner with a greater potency than the H2L ligand and the free copper ion displaying even higher antitumor activity than the well-known anticancer metallodrug cisplatin. CONICET (PIP 11220130100651CO and PIP 0034), UNLP (111/X673) and ANPCyT (PICT 2014-2223) of Argentina. Consejería de Educación CyL and FFEDER BU076U16, BU022G18 and Ministerio de Economía y Competitividad CTQ2016-75023-C2-1-P and CTQ2015-70371-REDTMetDrugs Network (Spain) |
| Databáze: | OpenAIRE |
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