Search results for "Roche"

showing 10 items of 2666 documents

Transmembrane electrochemistry of erythrocytes: Direct electrochemical test for detecting hemolysis in whole blood

2016

A rapid method for detecting hemolysis in whole blood based on a direct electrochemical assay either in venous blood and finger blood, respectively at glassy carbon and screen-printed graphite electrodes is described. The presence of hemolysis is detected from characteristic voltammetric signatures associated to Fe-heme units in healthy and hemolyzed erythrocytes. The voltammetric response of blood was also investigated using scanning electrochemical microscopy (SECM) and scanning tunneling microscopy (STM) and involved transmembrane electrochemistry of erythrocytes superimposed to molecular electrochemistry of heme-containing proteins and heme fragments in the plasma. Voltammetric testing …

Analytical chemistry02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesScanning electrochemical microscopyBlood plasmaMaterials ChemistrymedicineElectrochemistryElectrical and Electronic EngineeringInstrumentationWhole bloodHemolysis indexDetection limitChromatographyChemistryMetals and AlloysVenous blood021001 nanoscience & nanotechnologyCondensed Matter Physicsmedicine.diseaseHemolysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsVenous bloodFinger blood0210 nano-technology
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X-ray analysis on the nanogram to microgram scale using porous complexes

2012

X-ray single-crystal diffraction (SCD) analysis has the intrinsic limitation that the target molecules must be obtained as single crystals. Here we report a protocol for SCD analysis that does not require the crystallization of the sample. In our method, tiny crystals of porous complexes are soaked in a solution of the target, such that the complexes can absorb the target molecules. Crystallographic analysis clearly determines the absorbed guest structures along with the host frameworks. Because the SCD analysis is carried out on only one tiny crystal of the complex, the required sample mass is of the nanogram–microgram order. We demonstrate that as little as about 80 nanograms of a sample …

Analytical chemistryCrystallography X-RayMass spectrometryHigh-performance liquid chromatographyAbsorptionlaw.inventionCrystallawAnimalsNanotechnologyMoleculeCrystallizationta116Biological ProductsMultidisciplinaryChemistryMicrochemistryAnalytic Sample Preparation MethodsPoriferaCharacterization (materials science)AlkynesFatty AlcoholsAbsorption (chemistry)CrystallizationPorous mediumPorosityNature
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First signals of electrochemically oxidized species of TTF and TMT-TTF : a study by in situ spectroelectrochemical FTIR and DFT calculations

2003

A first study by in situ FTIR spectroelectrochemistry of TTF and TTM-TTF has been undertaken. The oxidation, in this case, is caused only by electrochemistry, which constitutes a clear advantage over chemical oxidation since no side products are present in the solution. In this context, we obtained the signals of neutral, radical cation, and dication species of TTF and TTM-TTF. The experimental conditions were chosen in order to avoid the possible formation of π-dimer species and to obtain a satisfactory signal-to-noise ratio. A weak signal was detected for TTF and a stronger one for TTM-TTF. The changes induced by the oxidation process in the IR spectra of TTF and TTM-TTF have been analyze…

Analytical chemistryGeneral Physics and AstronomyInfrared spectroscopyContext (language use)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesFourier transform spectroscopy0104 chemical sciencesDicationchemistry.chemical_compoundRadical ionchemistryPhysical chemistryDensity functional theoryPhysical and Theoretical Chemistry0210 nano-technologyTetrathiafulvalene
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Thermodynamic Study of Small Hydrophobic Ions at the Water–Lipid Interface

2001

Abstract The thermodynamics of binding of two small hydrophobic ions such as norharman and tryptophan to neutral and negatively charged small unilamellar vesicles was investigated at pH 7.4 using fluorescence spectroscopy. Vesicles were formed at room temperature from dimyristoyl phosphatidylcholine (DMPC) or DMPC/dimyristoylphosphatidic acid and DMPC/dimyristoylphosphatidylglycerol. The changes in fluorescence properties were used to obtain association isotherms at variable membrane surface negative charge and at different ionic strengths. The binding of both ions was found to be quantitatively enhanced as the percentage of negative phospholipid increases in the membrane. Also, a decrease …

Analytical chemistryPhospholipidPhosphatidic AcidsIonic bondingBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryIon bindingElectrochemistryLipid bilayerUnilamellar LiposomesIonsChromatographyVesicleTryptophanBinding constantSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPartition coefficientHarminechemistryPartition equilibriumThermodynamicslipids (amino acids peptides and proteins)DimyristoylphosphatidylcholineHydrophobic and Hydrophilic InteractionsCarbolinesJournal of Colloid and Interface Science
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A Supramolecularly-Caged Ionic Iridium(III) Complex Yielding Bright and Very Stable Solid-State Light-Emitting Electrochemical Cells

2008

A new iridium(III) complex showing intramolecular interligand pi-stacking has been synthesized and used to improve the stability of single-component, solid-state light-emitting electrochemical cell (LEC) devices. The pi-stacking results in the formation of a very stable supramolecularly caged complex. LECs using this complex show extraordinary stabilities (estimated lifetime of 600 h) and luminance values (average luminance of 230 cd m-2) indicating the path toward stable ionic complexes for use in LECs reaching stabilities required for practical applications.

Analytical chemistrySolid-statechemistry.chemical_elementIonic bondingGeneral ChemistryPhotochemistryBiochemistryLuminanceCatalysisElectrochemical cellColloid and Surface ChemistrychemistryIntramolecular forceIridiumJournal of the American Chemical Society
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Graphene and ionic liquids new gel paste electrodes for caffeic acid quantification

2015

Abstract Graphene/ionic liquids nanocomposite gels were synthesized by an electrochemical etching approach and fully characterized under a morphological and structural point of view. For this purpose, several analytical techniques were applied, as HR-TEM/EDX (High Resolution-Transmission Electron Microscopy/Energy Dispersive X-Ray Analysis); FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-Ray Analysis); XPS (X-Ray Photoelectron Spectroscopy); FT-IR (Fourier Transform-Infrared Spectroscopy) and electrochemical techniques. After the characterization study, nanocomposite-gel paste electrodes were assembled, exhibiting a selective and specific detection toward the ca…

Analytical chemistrySurfaces Coatings and FilmAnti-oxidant agentsCondensed Matter PhysicAnti-oxidant agentIonic liquidElectrochemistrylaw.inventionNanocompositeschemistry.chemical_compoundX-ray photoelectron spectroscopylawgraphene Ionic liquids; nanocomposites; electrochemistry; caffeic acid; anti-oxidant agentsMaterials ChemistryElectrochemistryMoleculeElectrical and Electronic EngineeringInstrumentationSettore CHIM/02 - Chimica FisicaMaterials Chemistry2506 Metals and AlloySettore CHIM/03 - Chimica Generale e InorganicaDetection limitCaffeic acidNanocompositeNanocompositeGrapheneElectronic Optical and Magnetic MaterialMetals and AlloysCondensed Matter Physicsgraphene Ionic liquidsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonic liquidschemistryChemical engineeringIonic liquidElectrode2506Graphene
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Application of a Novel Refinement Method for Accurate Determination of Chemical Diffusion Coefficients in Electroactive Materials by Potential Step T…

2005

We describe application of a novel refinement method for an accurate determination of the chemical diffusion coefficient, D, and the generalized kinetic parameter, A, from experimental potentiostatic intermittent titration technique (PITT) data suited for a variety of electrochemically doped electroactive polymers and inorganic intercalation host materials. The proposed, simple, two-step refinement procedure, based on earlier derived analytical expressions for the PITT response, is exemplified by the analysis of chronoamperometric responses to small-amplitude potential perturbation for p- and n-doped poly(fluorenone-bithiophene) (PFDOBT-HH) thin film electrode. The initial p-doping and the …

Analytical chemistryThermodynamics02 engineering and technology010402 general chemistryKinetic energy01 natural sciencesSolution of Schrödinger equation for a step potential[CHIM.ANAL]Chemical Sciences/Analytical chemistryMaterials ChemistryElectrochemistryElectroactive polymers[CHIM]Chemical SciencesDiffusion (business)Ohmic contactComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationRenewable Energy Sustainability and the EnvironmentTime constantPolymer021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.POLY]Chemical Sciences/PolymerschemistryElectrode0210 nano-technology
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Investigation into the reaction of (t-BuC5H4)2Nb(η2-Te2)H with CH3Li: Hydride abstraction versus telluride methylation

2007

Abstract The reaction of [ Cp 2 ′ Nb ( Te 2 ) H ] ( 1 ) (Cp′ =  t -BuC 5 H 4 ) with CH 3 Li in THF was examined by variable temperature 1 H NMR, ESR and mass spectroscopic means. From these methods it is evident that the diamagnetic compounds [ Cp 2 ′ NbH 2 ( TeCH 3 ) ] ( 2 ) and [ Cp 2 ′ Nb ( Te ) CH 3 ] ( 3 ) as well as the paramagnetic compound [ Cp 2 ′ Nb ( TeCH 3 ) 2 ] ( 4 ) form simultaneously. In the subsequent reaction of the intermediate solution with [Co 2 (CO) 8 ] compound 4 was consumed and the compound [ Cp 2 ′ Nb ( μ - TeCH 3 ) 2 Co(CO) 2 ] ( 5 ) formed in good yield. Complex 5 was characterized by IR and variable temperature 1 H NMR spectroscopies. Electrochemical two-electro…

Analytical chemistrychemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciencesInorganic ChemistryParamagnetismchemistry.chemical_compoundcarbonyl ligandsTelluridetelluriumMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistryHydride[ CHIM.COOR ] Chemical Sciences/Coordination chemistrycobalt0104 chemical sciencesCrystallographychemistryelectrochemistryYield (chemistry)Proton NMRTelluriumniobiumCobalt
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Polyacrylonitrile block copolymers for the preparation of a thin carbon coating around TiO2 nanorods for advanced lithium-ion batteries.

2013

Herein, a new method for the realization of a thin and homogenous carbonaceous particle coating, made by carbonizing RAFT polymerization derived block copolymers anchored on anatase TiO2 nanorods, is presented. These block copolymers consist of a short anchor block (based on dopamine) and a long, easily graphitizable block of polyacrylonitrile. The grafting of such block copolymers to TiO2 nanorods creates a polymer shell, which can be visualized by atomic force microscopy (AFM). Thermal treatment at 700 °C converts the polyacrylonitrile block to partially graphitic structures (as determined by Raman spectroscopy), establishing a thin carbon coating (as determined by transmission electron m…

AnataseMaterials sciencePolymers and PlasticsSurface PropertiesAcrylic Resins02 engineering and technologyThermal treatmentLithium010402 general chemistry01 natural scienceschemistry.chemical_compoundElectric Power SuppliesMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationComposite materialParticle Sizechemistry.chemical_classificationIonsTitaniumNanotubesMolecular StructureOrganic ChemistryPolyacrylonitrileTemperaturePolymerElectrochemical Techniques021001 nanoscience & nanotechnologyCarbon0104 chemical scienceschemistryTransmission electron microscopyNanorod0210 nano-technologyMacromolecular rapid communications
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Stabilizing nanostructured lithium insertion materials via organic hybridization: A step forward towards high-power batteries

2014

Abstract Herein, we present the electrochemical characterization of carbon-coated TiO 2 nanorods, obtained by carbonizing RAFT (reversible addition fragmentation chain transfer) polymerization derived block copolymers anchored on anatase TiO 2 nanorods. These carbon-coated TiO 2 nanorods show an improved electrochemical performance in terms of first cycle reversibility, specific capacity, cycling stability, and high rate capability. More importantly, however, the structural disordering observed in the uncoated TiO 2 nanorods by means of galvanostatic and potentiodynamic cycling as well as ex situ XRD analysis, does not occur for the carbon-coated material. Preventing this structural disorde…

AnataseMaterials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementChain transferElectrochemistryPolymerizationchemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationLithiumNanorodElectrical and Electronic EngineeringPhysical and Theoretical ChemistryJournal of Power Sources
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