Search results for "Química Analítica"

showing 10 items of 98 documents

Triplet exciplexes as energy transfer photosensitisers

2006

Experimental evidence is provided for the occurrence of triplet–triplet energy transfer from benzoylthiophene–indole exciplexes to naphthalenes with a remarkable stereodifferentiation; chiral recognition is also observed in the decay of the generated naphthalene triplets. Perez Prieto, Julia, Julia.Perez@uv.es ; Galian, Raquel Eugenia, Raquel.Galian@uv.es ; Morant Miñana, Maria Carmen, Maica.Morant@uv.es

Chiral recognitionStereochemistryEnergy transferUNESCO::QUÍMICAStereodifferentiationBenzoylthiophenePhotochemistry:QUÍMICA [UNESCO]CatalysisTriplet exciplexeschemistry.chemical_compoundMaterials ChemistryTriplet exciplexes ; Energy transfer ; Photosensitisers ; Benzoylthiophene ; Stereodifferentiation ; Chiral recognition ; NaphthalenePhysics::Chemical PhysicsNaphthaleneUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPhotosensitiserschemistryEnergy transferCeramics and Composites:QUÍMICA::Química analítica [UNESCO]Naphthalene
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Enantiomeric separation of chiral phenoxy acid herbicides by electrokinetic chromatography. Application to the determination of analyte-selector appa…

2001

The enantiomeric resolution of chiral phenoxy acid herbicides was performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC). A systematic evaluation of several neutral and charged cyclodextrins was made. Among the cyclodextrins tested, (2-hydroxy)propyl beta-cyclodextrin (HP-beta-CD) was found to be the most appropriate for the enantioseparation of phenoxy acids. The influence of some experimental conditions, such as nature and pH of the background electrolyte, chiral selector concentration, and temperature, on the enantiomeric separation of phenoxy acids was also studied. The use of a 50 mM electrolyte solution in ammonium formate at pH 5 and a temperat…

CienciaAnalyteElectrokinetic chromatographyResolution (mass spectrometry)ScienceChemistry analytic and technicalClinical BiochemistryElectrolytePhenoxy acid herbicidesBiochemistryAnalytical ChemistryElectrolyteschemistry.chemical_compoundElectrokinetic phenomenaTwo temperatureCIENCIAAmmonium formateOrganic chemistrychemistry.chemical_classificationChromatographyCyclodextrinsChromatographyCyclodextrinHerbicidesChemistryPhenyl Ethersbeta-CyclodextrinsTemperatureStereoisomerismQuímica analítica e industrialSCIENCEHydrogen-Ion Concentration2-Hydroxypropyl-beta-cyclodextrinSolutionsPropionatesEnantiomerELECTROPHORESIS
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Fast enantiomeric separation of uniconazole and diniconazole by electrokinetic chromatography using an anionic cyclodextrin: application to the deter…

2000

The enantiomeric resolution of the fungicides uniconazole and diniconazole was performed using electrokinetic chromatography with cyclodextrins as pseudostationary phase (CD-EKC). A systematic evaluation of several chiral selectors was made. The anionic derivative carboxymethylated-gamma-cyclodextrin (CM-gamma-CD) was found to be the most appropriate for the enantioseparation of fungicides among all cyclodextrins tested. The influence of some experimental conditions such as nature and buffer pH, chiral selector concentration, and temperature on the enantiomeric separation of the compounds studied was also investigated. The use of a 50 mM phosphate buffer (pH 6.5) containing 5 mM CM-gamma-CD…

CienciaAnalyteResolution (mass spectrometry)Electrokinetic chromatographyScienceClinical BiochemistryUniconazoleChemistry analytic and technicalDerivativeBiochemistryAnalytical ChemistryElectrokinetic phenomenaPhase (matter)CIENCIAchemistry.chemical_classificationCyclodextrinsChromatographyCyclodextrinElectrophoresis CapillaryStereoisomerismQuímica analítica e industrialSCIENCETriazolesDiniconazoleFungicides IndustrialUniconazolechemistryIndicators and ReagentsEnantiomer
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Specific interaction of citrate with bis(fluorophoric) bibrachial lariat aza-crown in comparison with the other components of the Krebs cycle

2006

Clares Garcia, M. Paz, M.Paz.Clares@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Soriano Soto, Concepcion, Concepcion.Soriano@uv.es ; Tejero Toquero, Roberto, Roberto.Tejero@uv.es

Citrate ; Krebs cycle ; Fluorescence ; NaphthaleneUNESCO::QUÍMICACrown (botany)UNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryFluorescenceMedicinal chemistry:QUÍMICA [UNESCO]CatalysisFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCitric acid cyclechemistry.chemical_compoundchemistryBiochemistryMaterials ChemistryCeramics and Composites:QUÍMICA::Química analítica [UNESCO]CitrateKrebs cycleThe Krebs CycleNaphthaleneNaphthalene
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Two are not always better than one: ligand optimisation for long-living light-emitting electrochemical cells

2009

The complex [Ir(ppy)2(dpbpy)][PF6] (Hppy = 2-phenylpyridine, dpbpy = 6,6'-diphenyl-2,2'-bipyridine) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs); the complex exhibits two intramolecular face-to-face π-stacking interactions and long-lived LECs have been constructed; the device characteristics are not significantly improved in comparison to analogous LECs with 6-phenyl-2,2'-bipyridine. Costa Riquelme, Ruben Dario, Ruben.Costa@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es ; Bolink, Henk, Henk.Bolink@uv.es

Complex ; 2-phenylpyridine ; LECs ; Light-emitting electrochemical cellsLigandUNESCO::QUÍMICALight-emitting electrochemical cellsUNESCO::QUÍMICA::Química analíticaLECsMetals and AlloysNanotechnologyGeneral ChemistryElectroluminescence:QUÍMICA [UNESCO]Combinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsElectrochemical cellchemistry.chemical_compoundchemistryComplexIntramolecular force:QUÍMICA::Química analítica [UNESCO]Materials ChemistryCeramics and Composites2-phenylpyridine2-PhenylpyridineChemical Communications
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Enantio- and diastereocontrol in intermolecular cyclopropanation reaction of styrene catalyzed by dirhodium(II) complexes with bulky ortho-metalated …

2004

Enantiomerically pure dirhodium(II) complexes with ortho-metalated p-substituted aryl phosphines have been shown to be enantio- and diastereoselective in the cyclopropanation of styrene by ethyl diazoacetate. Enantioselectivities up to 91% and diastereoselectivities up to 90% are observed for ethyl cis-2-phenylcyclopropanecarboxylate. Estevan Estevan, Francisco, Francisco.Estevan@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Lloret Fillol, Julio, Julio.Lloret@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es ; Ubeda Picot, M Angeles, Angeles.Ubeda@uv.es ; Vila Gomez, Jaume Llorenc, Jaume.Vila@uv.es

CyclopropanesModels MolecularReactionPhosphinesCyclopropanationUNESCO::QUÍMICAIntermolecularCrystallography X-RayMedicinal chemistryHydrocarbons Aromatic:QUÍMICA [UNESCO]CatalysisStyrenesCatalysisStyrenechemistry.chemical_compoundEthyl diazoacetateOrganometallic CompoundsMaterials ChemistryOrganic chemistryRhodiumIntermolecular ; Reaction ; Dirhodium ; Phosphines ; CyclopropanationMolecular StructureCyclopropanationArylIntermolecular forceUNESCO::QUÍMICA::Química analíticaMetals and AlloysStereoisomerismGeneral MedicineGeneral ChemistryDirhodiumSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCyclization:QUÍMICA::Química analítica [UNESCO]Ceramics and Composites
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White-light phosphorescence emission from a single molecule: application to OLED.

2009

A simple mononuclear cyclometallated iridium(III) complex exhibits white photo- and electro- luminescence in the wavelength range from 440 to 800 nm, which originates from a single emitting excited state of mixed character. Bolink Henk, Henk.Bolink@uv.es ; Coronado Miralles, Eugenio, Eugenio.Coronado@uv.es

DesignLuminescenceUNESCO::QUÍMICAAb initioColorchemistry.chemical_elementEfficiency010402 general chemistryPhotochemistry:QUÍMICA [UNESCO]01 natural sciencesCatalysisCopolymerIridium ComplexesMaterials ChemistryOLEDMoleculeIridiumDiodeEmitting DevicesMononuclear cyclometallated iridiumPhosphorescence010405 organic chemistryChemistrybusiness.industryUNESCO::QUÍMICA::Química analíticaMetals and AlloysAb-InitioGeneral ChemistryDiodes0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBlueOLEDExcited stateGreen:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesOptoelectronicsMononuclear cyclometallated iridium ; Luminescence ; Phosphorescence ; OLEDLuminescencePhosphorescencebusinessChemical communications (Cambridge, England)
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Bio-metal-organic frameworks for molecular recognition and sorbent extraction of hydrophilic vitamins followed by their determination using HPLC-UV

2020

A bio-metal-organic framework (bio-MOF) derived from the amino acid L-serine has been prepared in bulk form and evaluated as sorbent for the molecular recognition and extraction of B-vitamins. The functional pores of bio-MOF exhibit high amounts of hydroxyl groups jointly directing other supramolecular host-guest interactions thus providing the recognition of B-vitamins in fruit juices and energy drinks. Single-crystal X-ray diffraction studies reveal the specific B-vitamin binding sites and the existence of multiple hydrogen bonds between these target molecules and the framework. It offered unique snapshots to accomplish an efficient capture of these solutes in complex aqueous matrices. Fo…

Detection limitVitaminesSorbentChromatographySurface PropertiesUltraviolet RaysElutionChemistryHydrophilic interaction chromatography010401 analytical chemistryExtraction (chemistry)Supramolecular chemistryQuímica analítica010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryBegudesMolecular recognitionVitamin B ComplexAdsorptionSolid phase extractionParticle SizeHydrophobic and Hydrophilic InteractionsMetal-Organic FrameworksMicrochimica Acta
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Uncovering the metastable γ-Ag2WO4 phase: a joint experimental and theoretical study

2017

The synthesis of metastable solid phases is a pivotal starting point for innovative materials research. Here, we report the synthesis by means of a precipitation method of the metastable cubic γ-Ag2WO4 phase under ambient conditions. Different experimental techniques such as X-ray diffraction (XRD) with Rietveld refinement, field emission scanning electron microscopy (FE-SEM), micro-Raman/ultraviolet-visible (UV-vis) diffuse reflectance, photoluminescence spectroscopies, and differential scanning calorimetry (DSC) were employed. To complement the experimental data, the geometry, morphology, vibrational and electronic structure of γ-Ag2WO4 were characterized and evaluated using first-princip…

Electronic structureUncoveringGeneral Chemical EngineeringAnalytical chemistry02 engineering and technologyElectronic structure010402 general chemistry01 natural sciencesMolecular physicsMetastableCrystalsymbols.namesakeDifferential scanning calorimetryChemistryRietveld refinementGeneral ChemistryQuímica analítica021001 nanoscience & nanotechnologySurface energy0104 chemical sciencesEnamelssymbolsDensity of statesDensity functional theoryWulff construction0210 nano-technologyRaman spectroscopyCalculations
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nuevos desafíos en espectroscopia vibracional

2017

El principal objetivo de la Química Analítica Verde es la sustitución de metodologías contaminantes por otras más limpias, mediante:  La reducción de reactivos y disolventes empleados en el pre-tratamiento y análisis de las muestras.  Minimizar las cantidades y de la toxicidad de los compuestos empleados en las etapas de preparación y medida, especialmente mediante automatización y miniaturización.  El desarrollo de metodologías directas de análisis sin uso de reactivos o disolventes y que, por tanto, no generen desechos tóxicos ni peligrosos. Las técnicas espectroscópicas junto con el uso de la quimiometría pueden ser una buena alternativa a los métodos tradicionales, ya que se pueden r…

Espectroscopia vibracionalUNESCO::QUÍMICAQuímica Analítica VerdeMIRNIR:QUÍMICA [UNESCO]Raman
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