Search results for "SUBSTRATE"

showing 10 items of 1018 documents

Voltammetry of microparticles, scanning electrochemical microscopy and scanning tunneling microscopy applied to the study of dsDNA binding and damage…

2014

Abstract Microparticulate deposits of scorpiand-like azamacrocyclic receptors (L1–L4) attached to graphite electrodes provide distinctive voltammetric features in contact with aqueous DNA solutions at biological pH, denoting the formation of DNA surface complexes. This voltammetry allows for screening dsDNA, ssDNA and G-Quadruplex DNA using L4-modified electrodes. Scanning electrochemical microscopy and scanning tunneling microscopy examination of dsDNA fibers attached to the substrate electrode in contact with DMSO solutions containing ferrocene and receptor indicate that a synergic effect is exerted between electrochemically generated ferrocenium ion and the receptors so that they increas…

ChemistryGeneral Chemical EngineeringSubstrate (chemistry)DNA SolutionsAnalytical Chemistrylaw.inventionCrystallographyScanning electrochemical microscopychemistry.chemical_compoundFerrocenelawElectrodeElectrochemistryBiophysicsScanning tunneling microscopeBinding siteVoltammetryJournal of Electroanalytical Chemistry
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Adsorption of 3d Transition Elements on a TiO2(110) Surface.

2008

International audience; A first-principles study on the adsorption of 3d transition metal atoms on a stoichiometric TiO2(110) surface is reported. For all 3d elements except Cu, the most stable on-surface adsorption site is a site where the adatom binds to two twofold and one threefold surface oxygen atoms. For Ti, V, and Cr, however, a subsurface site, where the adatom substitutes a sixfold Ti atom, is more stable. The adatoms are oxidized in all cases. The charge transfer to the substrate is larger for the substitutional site than for the on-surface adsorption sites and decreases with atomic number along the 3d series. The relative stabilities of the adsorption sites are discussed in term…

ChemistryInorganic chemistry02 engineering and technologySubstrate (electronics)021001 nanoscience & nanotechnology01 natural sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsElectronegativityA-siteCrystallographyGeneral EnergyAdsorptionTransition metal0103 physical sciencesAtomAtomic numberPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyStoichiometry
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Die dimerisierung von endständigen α-hydroxyacetylenen mit rhodiumkomplexkatalysatoren

1978

Abstract The dimerisation of monosubstituted α-hydroxyacetylenes, which is catalysed by rhodium complexes, yields 1,4-disubstituted vinylacetylenes. The catalyst has been optimized for 3-methylbut-1-yn-3-ol as the substrate by using different ligands. Kinetic measurements were carried out with the monomers 3-methylbut-1-yn-3-ol, 3-methylpent-1-yn-3-ol and 1-ethynylcyclohexan-1-ol. In addition the rates of the dimerisation have been compared with those for a further series of α-hydroxyacetylenes. The by-products from the reaction of 3-methylbut-1-yn-3-ol with [(C 6 H 5 ) 3 P] 3 RhCl as catalyst were determined and the yields of the products compared with those of but-1-yn-3-ol and prop-1-yn-…

ChemistryOrganic ChemistrySubstrate (chemistry)chemistry.chemical_elementBiochemistryMedicinal chemistryCatalysisRhodiumInorganic Chemistrychemistry.chemical_compoundMonomerAcetyleneMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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MOCVD growth of CdTe on glass: analysis of in situ post-growth annealing

2004

Abstract In this paper, we analyse the growth by MOCVD of CdTe on glass substrates using in situ post-growth annealing. First, in order to perform a systematic study, polycrystalline layers of CdTe were deposited by MOCVD on glass substrates. The structure and morphology of the layers was investigated as a function of different growth parameters, temperature, VI/II precursor molar ratio and substrate position on the susceptor. An activation energy of Ek=20.7 kcal/mol was obtained from the experimental data. In order to better understand the process and the effects of different growth parameters, a numerical model that simulated the gas flow in the reactor, was developed. Secondly we analyse…

ChemistryScanning electron microscopeSubstrate (electronics)Activation energyCondensed Matter PhysicsCadmium telluride photovoltaicsAnnealing (glass)Inorganic ChemistryCrystallographysymbols.namesakeChemical engineeringMaterials ChemistrysymbolsCrystalliteMetalorganic vapour phase epitaxyRaman spectroscopyJournal of Crystal Growth
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Adsorption and activation of O2 at Au chains on MgO/Mo thin films

2010

We have investigated the adsorption of O(2) on Au(n) clusters (n = 1-6) supported by an ultra thin (3ML)MgO(001) film on Mo metal via density functional theory calculations. On thin films, these small clusters have chain like structures and their electronic states resemble 1D quantum well states. The Au(1-3) are charged by one electron whereas the larger Au(4-6) get two electrons from the substrate. This is confirmed both by the symmetries of the HOMO and LUMO states of the clusters and the Bader charge analysis. In contrast to the O(2) adsorption on gas-phase clusters, the adsorption energy of O(2) molecule does not show pronounced oscillations as a function of cluster size. The O(2) is ac…

ChemistryStereochemistryGeneral Physics and AstronomySubstrate (electronics)MetalCrystallographyAdsorptionvisual_artvisual_art.visual_art_mediumCluster (physics)MoleculeDensity functional theoryPhysical and Theoretical ChemistryThin filmHOMO/LUMOPhysical Chemistry Chemical Physics
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Relationships between fatty acid monolayer structure on the subphase and on solid substrates

1991

Abstract Docosanoic acid monolayers with known molecular packings on the water surface have been deposited on thin polymer films and then investigated using transmission electron diffraction at normal and tilted incidence. The diffraction patterns from monolayers deposited under all conditions investigated could be indexed as arising from the same conformationally disordered centred rectangular packing with molecules standing perpendicular to the substrate, although with a spread of unit cell parameters within and between each deposition condition significantly greater than the experimental error. This packing has been seen in monolayers on the water surface, but only under conditions compl…

ChemistryStereochemistryMetals and AlloysSurfaces and InterfacesSubstrate (electronics)Surface pressureSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyElectron diffractionPhase (matter)MonolayerMaterials ChemistryDeposition (phase transition)Phase diagramMonoclinic crystal systemThin Solid Films
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Assembly and Separation of Semiconductor Quantum Dot Dimers and Trimers

2011

Repeated precipitation of colloidal semiconductor quantum dots (QD) from a good solvent by adding a poor solvent leads to an increasing number of QD oligomers after redispersion in the good solvent. By using density gradient ultracentrifugation we have been able to separate QD monomer, dimer, and trimer fractions from higher oligomers in such solutions. In the corresponding fractions QD dimers and trimers have been enriched up to 90% and 64%, respectively. Besides directly coupled oligomers, QD dimers and trimers were also assembled by linkage with a rigid terrylene diimide dye (TDI) and separated again by ultracentrifugation. High-resolution transmission electron micrographs show that the …

ChemistrySurface PropertiesDimerAnalytical chemistryTrimerGeneral ChemistrySubstrate (electronics)PhotochemistryBiochemistryCatalysisSolventchemistry.chemical_compoundColloidColloid and Surface ChemistryMonomerSemiconductorsDiimideQuantum DotsDensity gradient ultracentrifugationParticle SizeDimerization
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Real-space observation of xenon adsorption and desorption kinetics on graphite (0001) by photoemission electron microscopy

2003

Abstract The growth and desorption of Xe monolayers on the basal plane of graphite has been investigated by real-space imaging using photoemission electron microscopy. Adsorption kinetics was studied at different substrate temperatures (39–65 K), corresponding to different growth modes. Coexisting phases showed up as different grey values in the image. Typical domain sizes of the 2D solid phases around 60 K are of the order of one to several μm. The domains exhibit an elongated shape with their long axis oriented preferentially parallel to step edges of the substrate. With increasing coverage the brightness of the domains increases, the 2D gas-phase regions shrink and finally disappear at h…

ChemistryThermal desorptionSurfaces and InterfacesSubstrate (electronics)Condensed Matter PhysicsMolecular physicsSurfaces Coatings and FilmsPhotoemission electron microscopyPhase (matter)DesorptionMonolayerMaterials ChemistryPhysical chemistryGraphitePhase diagramSurface Science
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Carotenoid binding sites in LHCIIb

2000

The major light-harvesting complex of photosystem II can be reconstituted in vitro from its bacterially expressed apoprotein with chlorophylls a and b and neoxanthin, violaxanthin, lutein, or zeaxanthin as the only xanthophyll. Reconstitution of these one-carotenoid complexes requires low-stringency conditions during complex formation and isolation. Neoxanthin complexes (containing 30–50% of the all-trans isomer) disintegrate during electrophoresis, exhibit a largely reduced resistance against proteolytic attack; in addition, energy transfer from Chl b to Chl a is easily disrupted at elevated temperature. Complexes reconstituted in the presence of either zeaxanthin or lutein contain nearly …

ChlorophyllLuteinPhotosynthetic Reaction Center Complex ProteinsPigment bindingLight-Harvesting Protein ComplexesXanthophyllsBiologyBinding CompetitiveBiochemistrySubstrate SpecificityLight-harvesting complexchemistry.chemical_compoundNeoxanthinZeaxanthinsTrypsinProtein PrecursorsCarotenoidPlant Proteinschemistry.chemical_classificationBinding SitesChlorophyll ALuteinPhotosystem II Protein Complexfood and beveragesPigments BiologicalPlantsbeta CaroteneCarotenoidseye diseasesZeaxanthinEnergy TransferchemistryBiochemistryXanthophyllElectrophoresis Polyacrylamide GelApoproteinsViolaxanthinEuropean Journal of Biochemistry
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Determination of major human cytochrome P450s activities in 96-well plates using liquid chromatography tandem mass spectrometry.

2007

At the early stage of drug discovery, thousands of new chemical entities (NCEs) may be screened before a single candidate can be identified for development. Evaluation of the effect of NCEs on human CYP450 enzyme activities is a key issue in pharmaceutical development as it may explain inter-subject variability, drug-drug interactions, non-linear pharmacokinetics and toxic effects. A liquid chromatography tandem mass spectrometry (HPLC-MS/MS) method has been developed for the fast and routine analysis of major human CYP450s enzyme activities (CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4) in primary hepatocyte cell cultures. The high sensitivity and selectivity of mass …

ChromatographyChemistryDrug discoveryCYP1A2Drug Evaluation PreclinicalGeneral MedicineToxicologyTandem mass spectrometryMass spectrometrySubstrate SpecificityPharmacokineticsCytochrome P-450 Enzyme SystemLiquid chromatography–mass spectrometryTandem Mass SpectrometryDrug DesignHepatocytesHumansCYP2A6Drug metabolismCells CulturedChromatography LiquidToxicology in vitro : an international journal published in association with BIBRA
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