Search results for "organometallic compound"

showing 10 items of 245 documents

An inconvenient influence of iridium(III) isomer on OLED efficiency.

2010

The recently reported heteroleptic cyclometallated iridium(III) complex [Ir(2-phenylpyridine)(2)(2-carboxy-4-dimethylaminopyridine)] N984 and its isomer N984b have been studied more in detail. While photo- and electrochemical properties are very similar, DFT/TDDFT calculations show that the two isomers have different HOMO orbital characteristics. As a consequence, solution processed OLEDs made using a mixture of N984 and isomer N984b similar to vacuum processed devices show that the isomer has a dramatic detrimental effect on the performances of the device. In addition, commonly used thermogravimetric analysis is not suitable for showing the isomerization process. The isomer could impact pe…

Thermogravimetric analysisInjectionMaterials scienceLightchemistry.chemical_elementTransportElectrochemistryPhotochemistryIridiumlaw.inventionPhosphorescent OledsInorganic ChemistryIsomerismComplexeslawOLEDElectrochemistryOrganometallic CompoundsDevicesIridiumDopantMolecular StructureConversionTime-dependent density functional theorychemistryElectrochemistry; Iridium; Isomerism; Molecular Structure; Organometallic Compounds; Light; Quantum TheoryGreenQuantum TheoryBipolar HostIsomerizationLight-emitting diodeLight-Emitting-Diodes
researchProduct

Structural basis and effect of copper(II) complexes with 4-oxo-thiazolidine ligands on DNA binding and nuclease activity

2020

Abstract Seven novel Copper(II) complexes, namely [Cu(Am4DHotaz)(H2O)2](ClO4) (1), [Cu(Am4DHotaz)(NO3)(MeOH)]·H2O (2), [Cu(Am4Motaz)2(H2O)](ClO4)2·0.83H2O (3), [Cu(Am4Motaz)2(NO3)]NO3·MeOH (4), [Cu(Am4Eotaz)2(NO3)]3(NO3)3·2H2O (5), [Cu(Am4Eotaz)2(ClO4)](ClO4) (6) and [Cu(Am4Eotaz)(ClO4)(H2O)](ClO4) (6a) (HAm4DHotaz = N′-(4-oxothiazolidin-2-ylidene)pyridine-2-carbohydrazonamide, Am4Motaz = N′-(3-methyl-4-oxothiazolidin-2-ylidene)pyridine-2-carbohydrazonamide and Am4Eotaz = N′-(3-ethyl-4-oxothiazolidin-2-ylidene)pyridine-2-carbohydrazonamide), have been successfully synthesized and characterized by several physicochemical techniques and, for 1–6 complexes, single crystal X-ray diffraction. Ha…

Thiazolidinechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundOrganometallic CompoundsGel electrophoresisNucleaseDeoxyribonucleasesbiology010405 organic chemistryHydrolysisDNACopperSquare pyramidal molecular geometry0104 chemical sciencesThiazolesCrystallographyTrigonal bipyramidal molecular geometrychemistrybiology.proteinSingle crystalCopperDNAJournal of Inorganic Biochemistry
researchProduct

Structure, magnetic properties and nuclease activity of pyridine-2-carbaldehyde thiosemicarbazonecopper(II) complexes.

2008

New complexes of formulae [Cu(HL 2 )(H 2 O)(NO 3 )](NO 3 ) ( 1 ), [{Cu(L 1 )(tfa)} 2 ] ( 2 ), [{Cu(L 1 )} 2 (pz)](ClO 4 ) 2 ( 3 ) and {[{Cu(L 1 )} 2 (dca)](ClO 4 )} n ( 4 ), where HL 1  = pyridine-2-carbaldehyde thiosemicarbazone, HL 2  = pyridine-2-carbaldehyde 4 N -methylthiosemicarbazone, Htfa = trifluoroacetic acid (CF 3 COOH), pz = pyrazine (C 4 H 4 N 2 ) and dca = dicyanamide [N(CN) 2 ] − , have been synthesized and characterized. The crystal structures of these compounds are built up of monomers ( 1 ), dinuclear entities with the metal centers bridged through the non-thiosemicarbazone coligand ( 2 and 3 ) and 1D chains of dimers ( 4 ). In all the cases, square–pyramidal copper(II) io…

ThiosemicarbazonesNucleasebiologyChemistryPyridineschemistry.chemical_elementCrystal structureDNACrystallography X-RayBiochemistryMagnetic susceptibilityCopperInorganic ChemistryMetalCrystallographychemistry.chemical_compoundMagneticsMonomervisual_artbiology.proteinvisual_art.visual_art_mediumOrganometallic CompoundsAntiferromagnetismSemicarbazoneCopperJournal of inorganic biochemistry
researchProduct

A study of electron transfer in Ru(dcbpy)2(NCS)2 sensitized nanocrystalline TiO2 and SnO2 films induced by red-wing excitation.

2008

Excited state dynamics and electron transfer from the Ru(dcbpy)2(NCS)2 (RuN3) sensitizer to semiconductor nanoparticles were studied using time-resolved femtosecond absorption spectroscopy. We found that excitation of the red wing of the absorption spectrum of the sensitizer populates the (3)MLCT state directly, both in solution and attached on semiconductor nanoparticle films. Electron injection is slowed down and becomes gradually less efficient as excitation moves towards red from the absorption maximum at 535 nm. At 675 nm the injection is non-exponential and characterized by 5, 30 and 180 ps time constants. The non-exponential electron injection observed is assigned to injection from a…

Time FactorsAbsorption spectroscopyPhotochemistrySurface PropertiesAnalytical chemistryGeneral Physics and AstronomyElectronsSensitivity and SpecificityRutheniumElectron transferOrganometallic CompoundsPhysical and Theoretical ChemistryTriplet stateAbsorption (electromagnetic radiation)Coloring AgentsTitaniumChemistrybusiness.industryLasersSpectrum AnalysisTin CompoundsMembranes ArtificialNanocrystalline materialNanostructuresKineticsSemiconductorSemiconductorsExcited stateFemtosecondbusinessThiocyanatesPhysical chemistry chemical physics : PCCP
researchProduct

Effect of tin and lead chlorotriphenyl analogues on fruit fly Drosophila hydei and liposomes membrane

2011

This article presents the results of a study investigating the biological activity of triphenyltin chloride (TPhT) and two metalloorganic compounds, triphenyllead chloride (TPhL) and triphenylmethane chloride (TPhC), in their interaction with model membranes and the living organisms of fruit flies Drosophila hydei. The study of model membranes (sonicated liposomes) was conducted using the electron spin resonance (ESR) spin probe technique, whereas the experiment on fruit flies involved investigating their viability on media containing the studied compounds. The test results clearly demonstrate that TPhT affects fruit flies more actively than TPhL (complete lethality after 7 days of culture …

Triphenyltin chlorideHealth Toxicology and MutagenesisToxicologyBiochemistryChloridechemistry.chemical_compoundOrganometallic CompoundsOrganotin CompoundsmedicineAnimalsLipid bilayerMolecular BiologyDrosophilaLiposomeTriphenylmethanebiologyCell MembranefungiElectron Spin Resonance SpectroscopyTrityl CompoundsGeneral Medicinebiology.organism_classificationMembraneLeadBiochemistrychemistryTinLiposomesModels AnimalDrosophila hydeiMolecular MedicineDrosophilamedicine.drugJournal of Biochemical and Molecular Toxicology
researchProduct

Effect of Chlorotriphenyl Derivatives of Sn and Pb upon Biophysical Properties of Membranes

2009

Biophysical activity of two twin organometallic compounds Triphenyltin chloride (TPhT) and Triphenyllead chloride (TPhL) in their interreaction with model membranes, as well as with yeast cellsSaccharomyces cerevisiae, was investigated. Four measurement methods were used in the experiments: two physical methods (spin probes method and the electric method); two biological methods (minimal inhibitory concentration /MIC/ and yeast survival test). It has been found that the activity of TPhT in interaction with model membranes and yeast cells is distinctly greater than that of TPhL. The activity manifests itself by considerable increase in the fluidity of the middle part of liposome bilayer, cha…

Triphenyltin chlorideTime FactorsArticle SubjectCell SurvivalHealth Toxicology and Mutagenesislcsh:BiotechnologySaccharomyces cerevisiaelcsh:MedicineSaccharomyces cerevisiaelcsh:Chemical technologylcsh:TechnologyBiophysical PhenomenaMembrane PotentialsCell membranechemistry.chemical_compoundlcsh:TP248.13-248.65GeneticsmedicineOrganometallic CompoundsOrganotin Compoundslcsh:TP1-1185Molecular BiologyLiposomebiologyChemistrylcsh:TBilayerCell Membranelcsh:RElectron Spin Resonance SpectroscopyLauric AcidsGeneral Medicinebiology.organism_classificationLauric acidYeastMembranemedicine.anatomical_structureBiochemistryLiposomesBiophysicsMolecular MedicineBiotechnologyResearch ArticleJournal of Biomedicine and Biotechnology
researchProduct

Synthesis, structural studies and reactivity of vanadium complexes with tridentate (OSO) ligand

2007

The direct reaction between [VCl(3)(thf)3] or [VO(OEt)3] and 2,2'-thiobis{4-(1,1,3,3-tetramethyl-butyl)phenol (tbopH(2)) leads to the formation of [V(2)(micro-tbop-kappa(3)O,S,O)2Cl(2)(CH(3)CN)(2)] (1).4CH(3)CN or [V(2)(micro-OEt)2(O)2(tbop-kappa(3)O,S,O)2] (2), respectively, in high yield. Compounds 1 and 2 were characterized by chemical and physical techniques including X-ray crystallography and variable temperature magnetic susceptibility studies (J = -29.1 cm(-1)) for 1. Complexes 1 and 2 were supported on MgCl2 and when activated with aluminium alkyls, were found to effectively polymerize ethene to produce polyethylene with a narrow molecular weight distribution M(w)/M(n) approximately…

Vanadium CompoundsLigandStereochemistrySpectrum AnalysisMagnesium ChlorideTemperatureVanadiumchemistry.chemical_elementCrystallography X-RayLigandsMedicinal chemistryMagnetic susceptibilityCatalysisCatalysisMolecular WeightInorganic ChemistrychemistryPolymerizationPolyethyleneYield (chemistry)NitrogenaseAluminum OxideOrganometallic CompoundsMolar mass distributionReactivity (chemistry)Dalton Trans.
researchProduct

Analysis of fluorescent MRI contrast agent behavior in the liver and thoracic aorta of mice.

2004

To characterize the behavior of magnetofluorescent products injected in mice intravenously.The magnetic resonance imaging (MRI) products were labelled with fluorescent molecules to examine the biodistribution process in vivo and observe them at the cellular level by means of confocal microscopy. Three-dimensional (3D) sequences of images were obtained by spectral analysis of sample preparations in a multiphoton confocal microscope and analyzed by the factor analysis of medical image sequence algorithm, which provides factor curves. Factor images are the result of image-processing methods that utilize information from emission spectra. Preparations are also screened in the counting mode to p…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingContrast MediaAorta ThoracicMiceMESH : Image CytometryMESH: Microscopy ConfocalMESH : FemaleMESH : Fluorescent DyesMESH: AnimalsMESH : Algorithms[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/Imaginghealth care economics and organizationsImage CytometryMice Inbred BALB CMicroscopy ConfocalMESH: Fluorescent DyesMESH: Staining and LabelingLiverMESH : MeglumineFemaleMESH : Organometallic CompoundsAlgorithmsMESH: Aorta ThoraciceducationMESH: Mice Inbred BALB CMESH: AlgorithmsMESH: MeglumineMESH : Staining and LabelingMeglumineMESH: Contrast MediaMESH : MiceOrganometallic CompoundsAnimalsMESH : Microscopy ConfocalMESH: MiceMESH : Mice Inbred BALB CFluorescent DyesMESH : Aorta ThoracicMESH : Contrast MediaStaining and LabelingMESH : LiverMESH: Organometallic CompoundsMESH : Xanthenes[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingXanthenesMESH: XanthenesMESH : AnimalsMESH: FemaleMESH: Image CytometryMESH: Liver
researchProduct

Quadruply-bonded dimolybdenum compounds: Reactivity towards TCNE. Structural evidences for the 1-D polymer [Mo2(O2 CCF3)4(TCNE)]∞

2005

cited By 3; International audience; Reaction of [Mo2(O2CR)4] (R = CF 3, 1) with TCNE in toluene affords the new compound [Mo2(O2CCF3)4 (TCNE)·6H5CH3 (2). The structure of 2 is built on [Mo2(O2 CCF3)4] fragments having the usual paddlewheel structure of 1 (Mo-Mo 2.1117(8) Å) and TCNE units. Each polynitrile moiety acts as a bridging ligand between two Mo2 fragments (Mo-N 2.875(4) Å) affording 1-D polymeric chains crossing in the crystal; the toluene molecules occupy the cavities between the chains. 13C NMR, IR and electrochemical data clearly show that formation of 2 does not involve electron density transfer from dimolybdenum fragment to the TCNE unit, which remains in 2 in its neutral stat…

chemical reactionReaction mechanismStereochemistryCoordination polymerGeneral Chemical EngineeringpolymerCrystal structureTetracyanoethylene010402 general chemistryligand01 natural scienceschemistry.chemical_compoundmolybdenumelectrochemical analysisMoietyMoleculetoluene[CHIM]Chemical SciencesReactivity (chemistry)electron transportchemical bondinfrared spectroscopychemical binding010405 organic chemistryChemistryarticleBridging ligandGeneral Chemistrycarbon nuclear magnetic resonance0104 chemical sciencesCrystallographychemical analysispolymerizationchemical structureorganometallic compound
researchProduct

Assembly and dichroism of a four-component halogen-bonded metal-organic cocrystal salt solvate involving dicyanoaurate(I) acceptors

2017

We describe the use of dicyanoaurate ions as linear ditopic metal–organic acceptors for the halogen bond-driven assembly of a dichroic metal–organic cocrystal based on azobenzene chromophores. Structural analysis by single crystal X-ray diffraction revealed that the material is a four-component solid, consisting of anticipated anionic metal–organic halogen-bonded chains based on dicyanoaurate ions, as well as complex potassium-based cations and discrete molecules of the crown ether 15-crown-5. Importantly, the structural analysis revealed the parallel alignment of the halogen-bonded chains required for dichroic behaviour, confirming that crystal engineering principles developed for the desi…

chemistry.chemical_classification010405 organic chemistryContext (language use)Dichroismorganometalliyhdisteet010402 general chemistryDichroic glassCrystal engineeringkiteet01 natural sciencesCocrystal0104 chemical scienceschemistry.chemical_compoundCrystallographyAzobenzenechemistryorganometallic compoundscrystalsMoleculePhysical and Theoretical Chemistryta116Crown etherFaraday Discussions
researchProduct