Search results for " Spectroscopy"

showing 10 items of 6851 documents

Soft-Chemical Growth ofγ-FeO(OH) Films on Self-Assembled Monolayers of Substituted Alkylthiols on Gold(111)

1999

Chemical engineeringAtomic force microscopyChemistryOrganic ChemistryInorganic chemistryMössbauer spectroscopySelf-assembled monolayerGeneral ChemistryTemplate synthesisCatalysisChemistry - A European Journal
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3D spectral imaging with synchrotron Fourier transform infrared spectro-microtomography

2013

We report Fourier transform infrared spectro-microtomography, a nondestructive three-dimensional imaging approach that reveals the distribution of distinctive chemical compositions throughout an intact biological or materials sample. The method combines mid-infrared absorption contrast with computed tomographic data acquisition and reconstruction to enhance chemical and morphological localization by determining a complete infrared spectrum for every voxel (millions of spectra determined per sample).

Chemical imagingmedicine.medical_specialtyMaterials scienceInfrared spectroscopyBiochemistryFourier transform spectroscopyPhysics::GeophysicsMicesymbols.namesakeImaging Three-DimensionalOpticsSpectroscopy Fourier Transform InfraredMicroscopyImage Processing Computer-AssistedmedicineAnimalsHumansFourier transform infrared spectroscopyMolecular BiologyEmbryonic Stem Cellsbusiness.industryX-Ray MicrotomographyCell BiologyWoodSpectral imagingPopulusFourier transformsymbolsbusinessChemical fingerprintingSynchrotronsHairBiotechnologyNature Methods
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Making Broad Proteome Protein Measurements in 1−5 min Using High-Speed RPLC Separations and High-Accuracy Mass Measurements

2005

The throughput of proteomics measurements that provide broad protein coverage is limited by the quality and speed of both the separations as well as the subsequent mass spectrometric analysis; at present, analysis times can range anywhere from hours (high throughput) to days or longer (low throughput). We have explored the basis for proteomics analyses conducted on the order of minutes using high-speed capillary RPLC combined through on-line electrospray ionization interface with high-accuracy mass spectrometry (MS) measurements. Short 0.8-microm porous C18 particle-packed 50-microm-i.d. capillaries were used to speed the RPLC separations while still providing high-quality separations. Both…

Chemical ionizationElectrosprayTime FactorsChromatographyProteomeChemistryElutionElectrospray ionizationAnalytical chemistryMass spectrometryMass SpectrometryPeptide FragmentsFourier transform ion cyclotron resonanceFourier transform spectroscopyAnalytical ChemistrySpectroscopy Fourier Transform InfraredAnimalsHumansTrypsinHydrophobic and Hydrophilic InteractionsIon cyclotron resonanceChromatography LiquidAnalytical Chemistry
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Synergies between Hyperpolarized NMR and Microfluidics: A Review

2021

Hyperpolarized nuclear magnetic resonance and lab-on-a-chip microfluidics are two dynamic, but until recently quite distinct, fields of research. Recent developments in both areas increased their synergistic overlap. By microfluidic integration, many complex experimental steps can be brought together onto a single platform. Microfluidic devices are therefore increasingly finding applications in medical diagnostics, forensic analysis, and biomedical research. In particular, they provide novel and powerful ways to culture cells, cell aggregates, and even functional models of entire organs. Nuclear magnetic resonance is a non-invasive, high-resolution spectroscopic technique which allows real-…

Chemical processNuclear and High Energy PhysicsMedical diagnosticMagnetic Resonance SpectroscopyPHYSICAL MANIPULATIONSComputer scienceProcess (engineering)MicrofluidicsMicrofluidicsFOS: Physical sciencesContext (language use)Nanotechnology02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistryLab-On-A-Chip DevicesPhysics - Chemical PhysicsHyperpolarization (physics)SpectroscopyChemical Physics (physics.chem-ph)021001 nanoscience & nanotechnologyMagnetic Resonance Imaging0104 chemical sciences0210 nano-technologyProgress in Nuclear Magnetic Resonance Spectroscopy
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1H, 13C, 15N NMR, ESI mass spectral and single crystal X-ray structural characterization of three spiro[pyrrolidine-2,3′-oxindoles]

2006

Abstract Three spiro[pyrrolidine-2,3′-oxindoles], 1,1′,2,2′,5′,6′,7′,7′a-octahydro-2-oxo-1′-phenyl-spiro[3H-indole-3,3′-[3H]-pyrrolizine]-2′-carboxylic acid methyl ester (1), 1,1′,2,2′,5′,6′,7′,7′a-octahydro-2-oxo-1′-nitro-2′-phenyl-spiro[3H-indole-3, 3′-[3H]-pyrrolizine] (2) and 1,1′,2,2′,5′,6′,7′,7′a-octahydro-2-oxo-1′-nitro-2′-(4″-chlorophenyl)-spiro[3H-indole-3,3′-[3H]-pyrrolizine] (3) have been synthesized and their 1H, 13C and 15N spectra assigned. The chemical shift assignments are based on Pulsed Field Gradient (PFG) Double Quantum Filter (DQF) 1H, 1H correlation spectroscopy (COSY), PFG 1H, 13C Heteronuclear Multiple Quantum Coherence (HMQC) and PFG 1H,X (X = 13C and 15N) Heteronuc…

Chemical shiftOrganic ChemistryAnalytical chemistryPyrrolidineSpectral lineAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryHeteronuclear moleculePulsed field gradientTwo-dimensional nuclear magnetic resonance spectroscopySingle crystalSpectroscopyMonoclinic crystal systemJournal of Molecular Structure
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Identity Double-Proton Transfer in (3Z)-3-Hydroxy-1,4-di(quinolin-2-yl)but-3-en-2-one

2003

Although there is a very fast (on the NMR timescale) double-proton transfer in (1Z,3Z)-3-hydroxy-4-quinolin-2-yl-1-quinolin-2(1H)-ylidenbut-3-en-2-one (the product of the condensation of ethyl oxalate with 2-lithiomethylquinoline), it is the only species present in chloroform solution. Comparison of the product of condensation of ethyl oxalate with 2-lithiomethyl derivatives of pyridine (recent studies) and quinoline (present studies) shows that benzoannulation considerably affects the tautomeric equilibrium. The observed changes are not only quantitative but also qualitative. Moreover, contrary to the proton transfer in the pyridine tautomers, this process is fast in the quinoline tautomer…

Chemical shiftOrganic ChemistryQuinolineAb initioGeneral ChemistryNuclear magnetic resonance spectroscopyTautomerCatalysisOxalateTransition statechemistry.chemical_compoundchemistryComputational chemistryPyridineChemistry - A European Journal
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Comparative NMR and IR spectral, X-ray structural and theoretical studies of eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides

2007

Abstract Eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides are characterized by NMR and IR spectroscopy. Single crystal X-ray structures for three congeners are reported. In addition, the transmission of substituent effects in conjugated double bond system of 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxide framework has been evaluated by calculating the correlations between selected 13C NMR chemical shifts and IR stretching wave numbers and Hammett constants of the substituents locating in the phenyl ring of the arylidene moiety.

Chemical shiftOrganic ChemistrySubstituentInfrared spectroscopyCarbon-13 NMRRing (chemistry)Analytical ChemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryComputational chemistryProton NMRMoietySingle crystalSpectroscopyJournal of Molecular Structure
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Mathematical Evaluation of Mössbauer Spectra

1978

As in many other spectroscopic methods, it is necessary in Mossbauer spectroscopy to determine the positions, intensities or areas of the absorption and emission lines as accurately as possible. In the case of poorly resolved or complex hyperfine spectra due to different chemical species or several lattice sites in the sample it is not possible to evaluate the Mossbauer spectra just by hand. In addition, often one is faced with the problem of taking into account cosine smearing effects (Sec. 4.2), thick absorbers associated with the calculation of the transmission integral (Sec. 3.5), magnetic or electric relaxation (Sec. 6.7), or delayed coincidence Mossbauer measurements (Sec. 3.5), which…

Chemical speciesMaterials scienceLattice (order)Complex lineMössbauer spectroscopyEmission spectrumAtomic physicsHyperfine structureSpectral lineCoincidence
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ChemInform Abstract: Coupled Semiconductor Systems for Photocatalysis. Preparation and Characterization of Polycrystalline Mixed WO3/WS2 Powders.

2010

Mixed WO3/WS2 powders were prepared by oxidation of WS2. The physical properties of the samples were characterized by X-ray diffraction, diffuse reflectance spectroscopy, and scanning electron microscopy; they were strongly dependent upon the time and temperature of oxidation. The chemical state and the elemental distribution of the sample surface were investigated by X-ray photoelectron spectroscopy. The photocatalytic results have showed that the aqueous suspensions of the mixed WO3/WS2 systems have significantly higher activities than pure WS2 and WO3 for the photodegradation of phenol. The enhanced performance can be related to the presence of heterojunctions WO3/WS2 on the single parti…

Chemical stateDiffuse reflectance infrared fourier transformChemical engineeringX-ray photoelectron spectroscopyChemistryScanning electron microscopePhotocatalysisGeneral MedicineCrystallitePhotodegradationMole fractionChemInform
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Cytotoxic Spirostane-Type Saponins from the Roots of Chlorophytum borivilianum

2009

Four new spirostane-type saponins named borivilianosides E-H (1-4) were isolated from an ethanol extract of the roots of Chlorophytum borivilianum together with two known steroid saponins (5 and 6). The structures of 1-4 were elucidated using mainly 2D NMR spectroscopic techniques and mass spectrometry. The cytotoxicity of borivilianosides F (2), G (3), and H (4) and three known compounds was evaluated using two human colon cancer cell lines (HT-29 and HCT 116).

Chemical structureIndiaPharmaceutical SciencePharmacologyPlant RootsAnalytical ChemistrySteroid SaponinsDrug DiscoverySpirostansHumansCytotoxic T cellMedicinal plantsCytotoxicityNuclear Magnetic Resonance BiomolecularAsparagaceaePharmacologyPlants MedicinalMolecular StructurebiologyTraditional medicineChemistryOrganic ChemistrySaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicHuman colon cancerComplementary and alternative medicineChlorophytum borivilianumMolecular MedicineDrug Screening Assays AntitumorTwo-dimensional nuclear magnetic resonance spectroscopyJournal of Natural Products
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