0000000000535940

AUTHOR

Marta Martínez-alonso

0000-0002-0931-5274

showing 6 related works from this author

Experimental and theoretical characterization of the strong effects on DNA stability caused by half-sandwich Ru(II) and Ir(III) bearing thiabendazole…

2020

Abstract: The synthesis and characterization of two half-sandwich complexes of Ru(II) and Ir(III) with thiabendazole as ancillary ligand and their DNA binding ability were investigated using experimental and computational methods. 1H NMR and acid–base studies have shown that aquo-complexes are the reactive species. Kinetic studies show that both complexes bind covalently to DNA through the metal site and non covalently through the ancillary ligand. Thermal stability studies, viscosity, circular dichroism measurements and quantum chemical calculations have shown that the covalent binding causes breaking of the H-bonding between base pairs, bringing about DNA denaturation and compaction. Addi…

Circular dichroismIridium(III)Base pairMolecular Dynamics SimulationIridium010402 general chemistry01 natural sciencesBiochemistryRutheniumInorganic ChemistryMetalchemistry.chemical_compoundMolecular dynamicsCoordination ComplexesThiabendazole010405 organic chemistryChemistryDNALigand (biochemistry)0104 chemical sciencesDNA destabilizationCrystallographyHalf-sandwichCovalent bondSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumProton NMRNucleic Acid ConformationDNARuthenium(II)
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Strong Influence of the Ancillary Ligand over the Photodynamic Anticancer Properties of Neutral Biscyclometalated IrIII Complexes Bearing 2-Benzoazol…

2018

In this paper, the synthesis, comprehensive characterization and biological and photocatalytic properties of two series of neutral IrIII biscyclometalated complexes of general formula [Ir(C^N)2(N^O)], where the N^O ligands are 2‐(benzimidazolyl)phenolate‐N,O (L1, series a) and 2‐(benzothiazolyl)phenolate‐N,O (L2, series b), and the C^N ligands are 2‐(phenyl)pyridinate or its derivatives, are described,. Complexes of types a and b exhibit dissimilar photophysical and biological properties. In vitro cytotoxicity tests conclusively prove that derivatives of series a are harmless in the dark against SW480 cancer cells (colon adenocarcinoma), but express enhanced cytotoxicity versus the same cel…

010405 organic chemistryLigandChemistrymedicine.medical_treatmentOrganic ChemistryPhotodynamic therapy2-arylazolesphotodynamictherapyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryanticancercomplexesCatalysis0104 chemical sciencesChemistryheterolepticneutraliridium(III)complexesmedicinephosphorescent complexesChemistry - A European Journal
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Highly Stable and Efficient Light-Emitting Electrochemical Cells Based on Cationic Iridium Complexes Bearing Arylazole Ancillary Ligands.

2017

A series of bis-cyclometalated iridium(III) complexes of general formula [Ir(ppy)2(N∧N)][PF6] (ppy− = 2-phenylpyridinate; N∧N = 2-(1H-imidazol-2-yl)pyridine (1), 2-(2-pyridyl)benzimidazole (2), 1-methyl-2-pyridin-2-yl- 1H-benzimidazole (3), 2-(4′-thiazolyl)benzimidazole (4), 1- methyl-2-(4′-thiazolyl)benzimidazole (5)) is reported, and their use as electroluminescent materials in light-emitting electrochemical cell (LEC) devices is investigated. [2][PF6] and [3][PF6] are orange emitters with intense unstructured emission around 590 nm in acetonitrile solution. [1][PF6], [4][PF6], and [5][PF6] are green weak emitters with structured emission bands peaking around 500 nm. The different photoph…

BenzimidazoleLigandchemistry.chemical_element02 engineering and technologyQuímica analíticaElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPyridineIridiumChemistry AnalyticPhysical and Theoretical ChemistryTriplet state0210 nano-technologyAcetonitrileHOMO/LUMOInorganic chemistry
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CCDC 1857871: Experimental Crystal Structure Determination

2018

Related Article: Marta Martínez-Alonso, Natalia Busto, Larry Danilo Aguirre, Leticia Berlanga, M. Carmen Carrión, José V. Cuevas, Ana M. Rodríguez, Arancha Carbayo, Blanca R. Manzano, Enrique Ortí, Félix A. Jalón, Begoña García, Gustavo Espino|2018|Chem.-Eur.J.|24|17523|doi:10.1002/chem.201803784

[2-(1H-benzimidazol-2-yl)phenolatato]-bis[35-difluoro-2-(pyridin-2-yl)phenyl]-iridium(iii) acetone solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1519073: Experimental Crystal Structure Determination

2017

Related Article: Marta Martínez-Alonso, Jesús Cerdá, Cristina Momblona, Antonio Pertegás, José M. Junquera-Hernández, Aránzazu Heras, Ana M. Rodríguez, Gustavo Espino, Henk Bolink, and Enrique Ortí|2017|Inorg.Chem.|56|10298|doi:10.1021/acs.inorgchem.7b01167

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(2-(pyridin-2-yl)phenyl)-(2-(13-thiazol-4-yl)-1H-benzimidazole)-iridium(iii) hexafluorophosphateExperimental 3D Coordinates
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CCDC 1519074: Experimental Crystal Structure Determination

2017

Related Article: Marta Martínez-Alonso, Jesús Cerdá, Cristina Momblona, Antonio Pertegás, José M. Junquera-Hernández, Aránzazu Heras, Ana M. Rodríguez, Gustavo Espino, Henk Bolink, and Enrique Ortí|2017|Inorg.Chem.|56|10298|doi:10.1021/acs.inorgchem.7b01167

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(1-methyl-2-(13-thiazol-4-yl)-1H-benzimidazole)-bis(2-(pyridin-2-yl)phenyl)-iridium(iii) hexafluorophosphateExperimental 3D Coordinates
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