Search results for "organometalli"

showing 10 items of 395 documents

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
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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
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Complexes of organometallic compounds

1966

Abstract The compounds (C2H5)2PbCl2, (C2H5)3PbCl and PbCl2 were studied by paper electrophoresis in aqueous LiCl solutions of various molarities. Determination was made of the formation of chloride complexes in which the electric charge was a function of ligand concentration in the solution. From the results of these experiments, and from a comparative examination of anion exchange data obtained in previous researches, useful information is obtained for determining the ligand concentrations relative to the preponderance of cationic, neutral and anionic complexes in the aqueous solutions. From this information it is possible to assume (C2H5)2PbCl42− and (C2H5)3PbCl32− as the fully coordinate…

TineInorganic chemistryHalideElectrolytePaper electrophoresisChlorideBiochemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundPolymer chemistrymedicineMaterials ChemistryPhysical and Theoretical ChemistryGroup 2 organometallic chemistryAqueous solutionChromatographyIon exchangeLigandOrganic ChemistryCationic polymerizationGeneral MedicineElectrophoresisPaper chromatographychemistryFluoridemedicine.drugJournal of Chromatography A
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Titanium Complexes Stabilized by a Sulfur‐Bridged Chelating Bis(aryloxo) Ligand as Active Catalysts for Olefin Polymerization

2004

The mixed-ligand complexes [Ti2(μ-OR)2(OR)2(κ3-tbop)2] (1a) for R = Me and (1b) R = Et were prepared by the reaction of Ti(OR)4 and H2tbop {H2tbop = 2,2′-thiobis[4-(1,1,3,3-tetramethylbutyl)phenol]} in methanol. Treatment of 1a and 1b with AlMe3 led to the substitution of terminal alkoxy groups to create the organometallic compounds [Ti2(μ-OR)2(κ3-tbop)2(Me)2] (2a) for R = Me and (2b) for R = Et. Controlled hydrolysis of 2b causes the evolution of methane and the formation of the titanoxane compounds [{Ti2(μ-OEt)2(κ3-tbop)2}2(μ-O)2]·2CH2Cl2 (3). Structures of 1a, 1b, 2a, 2b, and 3 were confirmed by NMR spectroscopy; 1b and 3 were further investigated with X-ray crystallography. Compounds 1a…

TitaniumEthyleneLigandSONuclear magnetic resonance spectroscopyCatalysisPolymerizationInorganic Chemistrychemistry.chemical_compoundO ligandschemistryPolymerizationPolymer chemistryAlkoxy groupChelationX‐ray diffractionGroup 2 organometallic chemistryAluminumEuropean Journal of Inorganic Chemistry
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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
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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
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Crystal structure of μ-oxido-1,1′κ2 O:O-bis{tetra-μ-oxido-1:2κ2 O:O;1:3κ2 O:O;2:3κ4 O:O-tris[1,2,3(η5)-penta­methyl­cyclo­penta­dien­yl]-trianglo-tri…

2015

The title polynuclear organometallic titanium(IV) oxide, [{Ti3(η5-​C5Me5)​3(μ-​O)​4}​2(μ-​O)​]​, exhibits two Ti3O4 cores bridged by an O atom located on a twofold axis. All metal centers present the typical three-​legged piano-​stool coordination environment, where one site is occupied by a pentamethylcyclopentadienyl ligand linked in an η5-​coordination fashion, while three bridging O atoms fill the other three sites.

Triscrystal structureorganometallicOxidechemistry.chemical_elementNanotechnologytitanium oxideCrystal structureMedicinal chemistryMetalchemistry.chemical_compoundGeneral Materials Sciencepentamethylcyclopentadienyl ligandCrystallographybiologyGeneral ChemistryQuímicaCondensed Matter Physicsbiology.organism_classificationData ReportsTitanium oxideChemistrychemistryQD901-999visual_artvisual_art.visual_art_mediumTetrapenta­methyl­cyclo­penta­dienyl ligandTitaniumActa Crystallographica Section E: Crystallographic Communications
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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.
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Sulfur Dioxide Oxidation Catalyzed by Photosensitized Ytterbium Diphthalocyanine

2008

Oxidation of SO2 into SO3 was found effectively catalyzed by photosensitized ytterbium diphthalocyanine, YbPc2 (Pc = phthalocyanine ligand, C32H16N8) when performed in air-saturated dimethylformamide (DMF) solution at 20 °C. The process follows according to a multi-step complex mechanism involving chemical induction as its driving force. Excitation energy of the sandwich molecular system in YbPc2 is used to promote the reaction by creating a reactive intermediate form of the ytterbium complex hosting up to eight SO2 molecules. The conversion of SO2 proved complete.

YtterbiumUV–Vis spectroscopyChemistryReactive intermediateExcited stateschemistry.chemical_elementHomogeneous catalysisGeneral ChemistryPhotochemistryHomogeneous catalysisCatalysisCatalysischemistry.chemical_compoundSulfur dioxidePhthalocyanineDimethylformamideMoleculeYtterbium diphthalocyaninePhotosensitizationOrganometallic chemistryCatalysis Letters
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Zirconium & Hafnium: Organometallic ChemistryBased in part on the article Zirconium & Hafnium: Organometallic Chemistry by Bernard Gautheron,…

2006

This review considers the main aspects of organometallic chemistry of zirconium and hafnium during the last 10 years. It is complementary to the first edition of Encyclopedia of Inorganic Chemistry. The material is presented in two major parts divided in five and three sections respectively. The first part is devoted to syntheses: the first section, by far the largest, covers in a systematic manner bis and mono cyclopentadienyl complexes with +4, +3, and +2 oxidation states and more especially constrained-geometry (CG) complexes, cationic complexes, and anionic or zwitterionic 18-electron complexes; unusual coordination geometries at carbon stabilized by group 4 metallocenes are presented i…

ZirconiumChemistryEnantioselective synthesisCationic polymerizationchemistry.chemical_elementHafniumCatalysischemistry.chemical_compoundCyclopentadienyl complexPolymerizationPolymer chemistryOrganic chemistryOrganic synthesisOrganometallic chemistry
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