Search results for "SPECTRA"

showing 10 items of 3542 documents

Correlation of high-field and zero- to ultralow-field NMR properties using 2D spectroscopy

2021

The field of zero- to ultralow-field (ZULF) nuclear magnetic resonance (NMR) is currently experiencing a rapid growth, owing to the progress in optical magnetometry, and also attractive features of ZULF NMR, such as low hardware cost and excellent spectral resolution achieved under ZULF conditions. In this work, an approach is proposed and demonstrated for simultaneous acquisition of ZULF-NMR spectra of individual 13C-containing isotopomers of chemical compounds in a complex mixture. The method makes use of fast field cycling, so that the spin evolution takes place at ZULF conditions, whereas signal detection is performed in a high-field NMR spectrometer. This method has excellent sensitivi…

Chemical Physics (physics.chem-ph)Materials science010304 chemical physicsField (physics)SpectrometerMagnetometerGeneral Physics and AstronomyFOS: Physical sciences010402 general chemistry01 natural sciencesMolecular physicsSpectral line0104 chemical sciencesIsotopomerslaw.inventionHeteronuclear moleculelawPhysics - Chemical Physics0103 physical sciencesCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistrySpectral resolutionSpectroscopy
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Tin-DNA complexes investigated by nuclear inelastic scattering of synchrotron radiation

2005

Nuclear inelastic scattering (NIS) of synchrotron radiation has been used to investigate the dynamics of tin ions chelated by DNA. Theoretical NIS spectra have been simulated with the help of density functional theory (DFT) calculations using 12 models for different binding sites of the tin ion in (CH3)Sn(DNAPhosphate)2. The simulated spectra are compared with the measured spectrum of the tin-DNA complex.

Chemical Physics (physics.chem-ph)Nuclear and High Energy PhysicsMaterials sciencenuclear inelastic scattering tin–DNASynchrotron radiationchemistry.chemical_elementFOS: Physical sciencesInelastic scatteringCondensed Matter PhysicsMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineIonchemistry.chemical_compoundCondensed Matter::Materials SciencechemistrySettore CHIM/03 - Chimica Generale E InorganicaPhysics - Chemical PhysicsPhysics::Accelerator PhysicsDensity functional theoryPhysical and Theoretical ChemistryTinNuclear ExperimentDNASettore CHIM/02 - Chimica Fisica
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A method for measurement of spin-spin couplings with sub-mHz precision using zero- to ultralow-field nuclear magnetic resonance.

2017

We present a method which allows for the extraction of physical quantities directly from zero- to ultralow-field nuclear magnetic resonance (ZULF NMR) data. A numerical density matrix evolution is used to simulate ZULF NMR spectra of several molecules in order to fit experimental data. The method is utilized to determine the indirect spin-spin couplings ($J$-couplings) in these, which is achieved with precision of $10^{-2}$--$10^{-4}$ Hz. The simulated and measured spectra are compared to earlier research. Agreement and precision improvement for most of the $J$-coupling estimates are achieved. The availability of an efficient, flexible fitting method for ZULF NMR enables a new generation of…

Chemical Physics (physics.chem-ph)Nuclear and High Energy PhysicsZero field NMRField (physics)ChemistryBiophysicsFOS: Physical sciences010402 general chemistryCondensed Matter Physics01 natural sciences7. Clean energyBiochemistrySpectral line0104 chemical sciences3. Good healthNMR spectra databaseMatrix (mathematics)Nuclear magnetic resonancePhysics - Chemical Physics0103 physical sciencesTransverse relaxation-optimized spectroscopy010306 general physicsSpin (physics)Two-dimensional nuclear magnetic resonance spectroscopyJournal of magnetic resonance (San Diego, Calif. : 1997)
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Measuring molecular parity nonconservation using nuclear-magnetic-resonance spectroscopy

2017

The weak interaction does not conserve parity and therefore induces energy shifts in chiral enantiomers that should in principle be detectable in molecular spectra. Unfortunately, the magnitude of the expected shifts are small and in spectra of a mixture of enantiomers, the energy shifts are not resolvable. We propose a nuclear magnetic resonance (NMR) experiment in which we titrate the chirality (enantiomeric excess) of a solvent and measure the diasteriomeric splitting in the spectra of a chiral solute in order to search for an anomalous offset due to parity nonconservation (PNC). We present a proof-of-principle experiment in which we search for PNC in the \textsuperscript{13}C resonances…

Chemical Physics (physics.chem-ph)PhysicsGeneral PhysicsChemical shiftphysics.chem-phFOS: Physical sciencesParity (physics)Nuclear magnetic resonance spectroscopyWeak interaction010402 general chemistry01 natural sciencesSpectral lineMathematical Sciences0104 chemical sciences3. Good healthPhysics - Chemical Physics0103 physical sciencesPhysical SciencesChemical SciencesPhysics::Atomic PhysicsAtomic physicsEnantiomer010306 general physicsEnantiomeric excessChirality (chemistry)
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Electric field enhanced water dissociation at the bipolar membrane junction from ac impedance spectra measurements

1998

Abstract Preliminary experimental results of the ac impedance spectra of a bipolar ion-exchange membrane are reported and interpreted on the basis of a previous theoretical model based on the Nernst–Planck/Poisson equations. It is shown that the experiments can provide valuable electrochemical information about the bipolar junction structure and the electric-field enhanced water dissociation phenomenon that occurs at this junction, although the high number of unknown parameters involved makes it difficult to obtain accurate values for the parameters characteristic of this phenomenon.

Chemical dissociationChemistryGeneral Chemical EngineeringAnalytical chemistryElectrochemistryMolecular physicsDissociation (chemistry)Analytical Chemistrysymbols.namesakeMembraneElectric fieldAc impedance spectraElectrochemistrysymbolsNernst equationElectrical impedanceJournal of Electroanalytical Chemistry
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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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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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Fourier transform nmr investigations of organotin compounds

1980

Abstract NMR spectra have been obtained for fiteen title compounds, mainly with R = Me. Tin chemical shifts were found to lie within the expected ranges, but to vary little with R or, apparently, with change in ring size. While the magnitute of 1 (SnSe) was as predicted, the of 1 (SnTe) was more than twice as large as that previously observed for (Me 3 Sn) 2 Te. In compounds Me 6 Sn( 3 X 3 , 2 J(SnMSn) varied systematically with variations in x, but within relatively narrow limits (195-250 Hz); a much more drastic variation was observed for Me 6 Sn 3 X 2 , possibly due to bond angle changes at Sn and X.

Chemical shiftOrganic ChemistryAnalytical chemistrychemistry.chemical_elementBiochemistryInorganic ChemistryRing sizeNMR spectra databasesymbols.namesakeMolecular geometryFourier transformchemistryMaterials ChemistrysymbolsPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Nitrogen-15 NMR Studies on Hydrazines. 2— Substituent Effect Analysis inortho-Substituted Phenylhydrazines and Anilines

1996

15N and 13C NMR spectra of some ortho-substituted phenylhydrazines were measured at natural isotope abundance in DMSO-d6 solutions. The substituent present exerts a larger effect on the chemical shift of the nitrogen atom directly bound to the aromatic ring (N-1), the second one (N-2) showing an attenuated trend of similar sign. Contrary to what observed for para and meta isomers, the cross-correlation between N-1 and N-2 SCS values of ortho-substituted phenylhydrazines is not satisfactory; on the other hand, N-1 SCSs show a reasonably good linear regression with the σR− constants. As expected, no correlation was found between N-1 and C-1 or H-1 SCS values. Correlations between 13C and 15N …

Chemical shiftPhenylhydrazinesSubstituentchemistry.chemical_elementNatural abundanceGeneral ChemistryCarbon-13 NMRRing (chemistry)PhotochemistryNitrogenMedicinal chemistrySpectral linechemistry.chemical_compoundchemistryGeneral Materials ScienceMagnetic Resonance in Chemistry
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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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