Search results for " Metal complex"

showing 10 items of 33 documents

2,2′:6′,2″-Terpyridine Trimethylplatinum(IV) Iodide Complexes as Bifunctional Halogen Bond Acceptors

2016

Three new organometallic trimethylplatinum(IV) iodide complexes of 2,2′:6′,2″-terpyridines have been synthesized and characterized by 1H NMR spectroscopy, mass spectrometry, elemental analysis, and single crystal X-ray diffraction analysis. The X-ray crystal structures of PtMe3I(L) complexes 1–3 {L for 1 = 4′-chloro-2,2′:6′,2″-terpyridine, 2 = 4′-(4-cyanophenyl)-2,2′:6′,2″-terpyridine, and 3 = 4′-(4-tolyl)-2,2′:6′,2″-terpyridine} reveal distorted octahedral coordination geometry of the platinum(IV) metal centers with bidentate coordination of the terpyridine ligands. Complexation of 1–3 with iodopentafluorobenzene (IPFB) afforded single-crystal structures of halogen bond (XB) complexes 1a–3…

chemistry.chemical_classificationDenticityHalogen bond010405 organic chemistryhalogen bondsIodideGeneral ChemistryCrystal structurehalogen bond acceptors010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencestransition metal complexes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryPyridineGeneral Materials ScienceTerpyridineBifunctionalta116Coordination geometryCrystal Growth & Design
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Studio dell'interazione di DNA con complessi di metalli di transizione

2014

G-quadruplextransition metal complexUv-ViDNACircular dichroismdicroismo circolareInorganic Chemistrymetal complexSchiff basechimica bioinorganicaintercalantiG4complessi metalliciChimica inorganicaSettore CHIM/03 - Chimica Generale E Inorganicametalli di transizioneBasi di SchiffG4-stabilizerBioinorganic Chemistryintercalator
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The Interaction of Small Molecules with Biomolecules

2014

The binding of small molecules with biological targets is associated to interesting chemical and biological properties of the resulting supramolecular systems. We have recently reported on the synthesis and characterization of cationic first row transition metal complexes and the study of their DNA binding properties, in aqueous solutions at neutral pH, essentially investigated by viscosimetry and spectroscopic techniques such as circular dichroism, absorption and fluorescence in the UV-visible wavelength range. Of course, such procedure cannot furnish atomic level details of the molecule-DNA interaction. Computational Chemistry may provide support for the interpretation of experimental dat…

Settore CHIM/03 - Chimica Generale E Inorganicatransition metal complexes DNA binding properties Molecular Dynamics G-quadruplexSettore CHIM/08 - Chimica Farmaceutica
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Antiproliferative Properties of a Few Auranofin-Related Gold(I) and Silver(I) Complexes in Leukemia Cells and their Interferences with the Ubiquitin …

2020

A group of triethylphosphine gold(I) and silver(I) complexes, structurally related to auranofin, were prepared and investigated as potential anticancer drug candidates. The antiproliferative properties of these metal compounds were assessed against two leukemia cell lines, i.e., CCRF-CEM and its multidrug-resistant counterpart, CEM/ADR5000. Interestingly, potent cytotoxic effects were disclosed for both series of compounds against leukemia cells, with IC50 values generally falling in the low-micromolar range, the gold derivatives being on the whole more effective than the silver analogues. Some initial structure-function relationships were drawn. Subsequently, the ability of the study compo…

ProteasesProteasome Endopeptidase ComplexAuranofinSilverleukemia cellsPharmaceutical Sciencemetal complexesantiproliferative propertiesArticleAnalytical ChemistryMetallcsh:QD241-44103 medical and health sciencesInhibitory Concentration 500302 clinical medicineGold Compoundslcsh:Organic chemistryCell Line TumorDrug DiscoverymedicineCytotoxic T cellHumansPhysical and Theoretical Chemistry030304 developmental biologyCell Proliferationproteasome inhibition0303 health sciencesLeukemiaChemistryUbiquitinOrganic Chemistryauranofinmedicine.diseaseauranofin metal complexes proteasome inhibition leukemia cells antiproliferative propertiesDrug Resistance MultipleLeukemiaProteasomeBiochemistryChemistry (miscellaneous)Drug Resistance Neoplasm030220 oncology & carcinogenesisvisual_artvisual_art.visual_art_mediumauranofin;metal complexes; proteasome inhibition; leukemia cells; antiproliferative propertiesMolecular MedicineGoldSelectivitymedicine.drugMolecules
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Ultrafast Relaxation Dynamics of Osmium−Polypyridine Complexes in Solution

2013

We present steady-state absorption and emission spectroscopy and femtosecond broadband photoluminescence up-conversion spectroscopy studies of the electronic relaxation of Os(dmbp)(3) (Os1) and Os(bpy)(2)(dpp) (Os2) in ethanol, where dmbp is 4,4'-dimethyl-2,2'-biypridine, bpy is 2,2'-biypridine, and dpp is 2,3-dipyridyl pyrazine. In both cases, the steady-state phosphorescence is due to the lowest (MLCT)-M-3 state, whose quantum yield we estimate to be <= 5.0 x 10(-3). For Os1, the steady-state phosphorescence lifetime is 25 ns. In both complexes, the photoluminescence excitation spectra map the absorption spectrum, pointing to an excitation wavelength-independent quantum yield. The ultrafa…

PhotoluminescenceAbsorption spectroscopyChemistryQuantum yieldPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyIntersystem crossingPhotoluminescence excitationSinglet statePhysical and Theoretical ChemistryTriplet statePhosphorescenceultrafast metal complex fluorescence upconversion osmium
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Flexible light-emitting electrochemical cells with single-walled carbon nanotube anodes

2016

Abstract In this work, we demonstrate flexible solution processed light emitting electrochemical cells (LECs) which use single-walled carbon nanotubes (SWCNTs) films as the substrate. The SWCNTs were synthesized by an integrated aerosol method and dry-transferred on the plastic substrates at room temperature. The addition of a screen printed poly (3,4-ethylene dioxythiophene) doped with poly (styrene sulfonate) (PEDOT:PSS) film onto the nanostructured electrode further homogenizes the surface and enlarges the work function, enhancing the hole injection into the active layer. By using an efficient phosphorescent ionic transition metal complex (iTMC) as the active material, efficacies up to 9…

Materials scienceLight-emitting electrochemical cellsFlexible devices02 engineering and technologySubstrate (electronics)Carbon nanotubeElectroluminescence010402 general chemistry01 natural sciencesElectrochemical celllaw.inventionBiomaterialsPEDOT:PSSlawSWCNTsMaterials ChemistryOLEDWork functionElectrical and Electronic Engineeringta114business.industryOLEDsGeneral ChemistryTransition metal complex021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesElectronic Optical and Magnetic MaterialsElectroluminescenceElectrodeOptoelectronics0210 nano-technologybusinessORGANIC ELECTRONICS
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Synthesis, characterization, cellular uptake and interaction with native DNA of a bis(pyridyl)-1,2,4-oxadiazole copper(II) complex

2010

The copper(II) complex of 3,5-bis(2'-pyridyl)-1,2,4-oxadiazole was synthesized and characterized. X-Ray crystallography revealed that the complex consists of a discrete [Cu(3,5-bis(2'-pyridyl)-1,2,4-oxadiazole)(2)(H(2)O)(2)](2+) cation and two ClO(4)(-) anions. The Cu(II) coordination sphere has a distorted octahedral geometry and each ligand chelates the copper ion through the N(4) nitrogen of the oxadiazole ring and the nitrogen of one pyridine moiety. The coordinated water molecules are in cis position and each of them is H-bonded to the 5-pyridyl nitrogen of the oxadiazole ligand and to an oxygen of the perchlorate anion. Biological assays showed that, despite the free ligand not being …

Models MolecularCircular dichroismCoordination sphereheterocylces metal complex DNA binders anti-tumoralsCell SurvivalPyridinesStereochemistrychemistry.chemical_elementOxadiazoleLigandsInorganic Chemistrychemistry.chemical_compoundPerchlorateCell Line TumorOctahedral molecular geometryOrganometallic CompoundsHumansOxadiazolesChemistryLigandDNASettore CHIM/06 - Chimica OrganicaCopperBinding constantCrystallographySettore CHIM/03 - Chimica Generale E InorganicaCopper
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Interaction of Novel Metal Complexes with DNA: Synthetic and Structural Aspects

2009

Metal ions bind to nucleic acids at various positions. This binding can be modulated by using metal complexes with appropriate ligands. Novel mono- and especially dinuclear metal complexes could be a powerful tool to detect rare, but still physiologically relevant, forms of DNA, e.g. the left-handed Z-DNA. In this review, our recent research activities in this area of bioinorganic chemistry are summarized. A special emphasis is laid on the synthetic challenges that arose upon the synthesis of the polyamine ligands. Further, some rather unusual approaches to elucidate the solution structure of copper bound to guanosine monophosphate with the help of pulsed EPR techniques like ENDOR and HYSC…

10120 Department of ChemistryMono- and dinuclear metal complexesMetal ions in aqueous solutionand dinuclear metal complexes1600 General ChemistrydnaBioinorganic chemistryZ-DNAMetalchemistry.chemical_compoundMono- and Dinuclear Metal ComplexeGuanosine monophosphate540 ChemistryQD1-999Pulsed EPRCrystal structureBioinorganic chemistryGeneral MedicineGeneral ChemistryZ-DNACombinatorial chemistrySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Chemistrychemistryvisual_artCrystal structuresNucleic acidvisual_art.visual_art_mediumMonoSynthetic ChemistryDNAZ
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THE INTERACTION OF NATIVE DNA WITH Ni(II), Cu(II) and Zn(II) COMPLEXES OF 5-TRIETHYL AMMONIUM METHYL SALICYLIDENE ORTHO-PHENYLENDIIMINE

2009

DNA binding Metal complexes Intercalators
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The solution behavior of dopamine in the presence of mono and divalent cations: A thermodynamic investigation in different experimental conditions

2021

The interactions of dopamine [2-(3,4-Dihydroxyphenyl)ethylamine, (Dop-)] with methylmercury(II) (CH3Hg+), magnesium(II), calcium(II), and tin(II) were studied in NaCl(aq) at different ionic strengths and temperatures. Different speciation models were obtained, mainly characterized by mononuclear species. Only for Sn2+ we observed the formation of binuclear complexes (M2L2 and M2LOH (charge omitted for simplicity)

Models MolecularCations DivalentDopaminePotentiometric titrationEnthalpyIonic bondingBiochemistryMicrobiologyArticleDivalentchemistry.chemical_compoundMetal complexesTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYSettore CHIM/01 - Chimica AnaliticaStability constantsMolecular Biologychemistry.chemical_classificationCatechol; Chemical speciation; Metal complexes; Sequestration; Stability constantsLigandHydrolysisOsmolar ConcentrationTemperatureSequestrationHydrogen-Ion ConcentrationQR1-502SolutionsKineticschemistrySpecific ion interaction theoryIonic strengthThermogravimetryCatecholPhysical chemistryThermodynamicsChemical speciationEthylamine
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