Search results for " Magnetic resonance"

showing 10 items of 2317 documents

Synthesis, characterization and thermal properties of nine quaternary dialkyldiaralkylammonium chlorides

2006

Abstract Nine R 2 R 2 ′ N + Cl − (R=benzyl, 2-methylbenzyl, 3-methylbenzyl, 4-methylbenzyl, 2-phenylethyl or 3-phenylpropyl; R′=ethyl or methyl) quaternary dialkyldiaralkylammonium chlorides were synthesized by treating dimethylformamide or diethylformamide with non-substituted or substituted arylalkyl (aralkyl) halide in the presence of sodium carbonate. The 1H NMR, 13C NMR spectroscopy, mass spectroscopy and elemental analysis were used to characterize the synthesized products. The crystal structures of six compounds were determined by X-ray single crystal diffraction. Four of the compounds crystallized in monoclinic space groups C2/c and P21/c (or P21/n), one in triclinic space group P−1…

ChemistryOrganic ChemistrySpace groupCrystal structureNuclear magnetic resonance crystallographyTriclinic crystal systemAnalytical ChemistryInorganic ChemistryCrystallographyOrthorhombic crystal systemSingle crystalSpectroscopyPowder diffractionMonoclinic crystal systemJournal of Molecular Structure
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Assessment of a single-acquisition imaging sequence for oxygen-sensitive (3)He-MRI.

2001

MRI of the lungs using hyperpolarized helium-3 (3He) allows the determination of intrapulmonary oxygen partial pressures (pO2). The need to separate competing processes of signal loss has hitherto required two different imaging series during two different breathing maneuvers. In this work, a new imaging strategy to measure pO2 by a single series of consecutive scans is presented. The feasibility of the method is demonstrated in three healthy human volunteers. Maps and histograms of intrapulmonary pO2 are calculated. Changes in the oxygen concentration of the inhaled gas mixture are well reproduced in the histograms. Monte Carlo (MC) simulations of the temporal evolution of 3He hyperpolariza…

ChemistryPartial PressureMonte Carlo methodHealthy subjectschemistry.chemical_elementrespiratory systemOxygenHeliumMagnetic Resonance ImagingOxygenNuclear magnetic resonanceIsotopesHistogramImage Processing Computer-AssistedHumansRadiology Nuclear Medicine and imagingLimiting oxygen concentrationComputer SimulationHyperpolarization (physics)Inhaled GasPulmonary VentilationLungMonte Carlo MethodLung functionMagnetic resonance in medicine
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Properties of methyl radical trapped in amorphous SiO2 and in natural SiO2-clathrate Melanophlogite

2013

Abstract We report an experimental investigation by electron paramagnetic resonance (EPR) on methyl radical (CH3 ) observed in γ-ray irradiated high-purity amorphous silicon dioxide (a-SiO2) and in a polycrystalline sample of Melanophlogite, a rare natural form of SiO2-clathrate. From the analysis of the EPR spectra we estimate the correlation time of the hindered rotational motion of CH3 molecules at T = 77 K in the two different materials. This physical quantity gives a quantitative measure of the freedom of motion of CH3 molecules trapped in the two solid systems, putting forward relevant information on the properties of the cavities/interstices in which the radicals are confined. In par…

ChemistryRadicalClathrate hydrateRadiation effectMethyl radicalSilicaCrystal structureengineering.materialCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsAmorphous solidlaw.inventionchemistry.chemical_compoundNuclear magnetic resonancelawChemical physicsMelanophlogiteMaterials ChemistryCeramics and CompositesengineeringMethyl radicalCrystalliteElectron paramagnetic resonanceClathrateElectron paramagnetic resonanceJournal of Non-Crystalline Solids
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Magnetic field-induced alignment of molecular rotor-shaped cyclophanes

2010

Molecular pinwheels consisting of dipolar substituted cyclophanes in solution can function as free microscopic rotors in the presence of a homogeneous static magnetic field B and a circularly polarized electric field E rotating on a plane containing B. Owing to the high magnetic anisotropy of [26](1,2,3,4,5,6)cyclophane and [36](1,2,3,4,5,6)cyclophane biased by strong ring currents, ∼1 in 105 molecules are expected to align with the C6 symmetry axis perpendicular to a magnetic field of 21 T. The magnetic-field-controlled alignment of rotor-shaped cyclophanes is insignificantly affected by nonpolar solvents, for example, toluene.

ChemistryRotor-shaped cyclophanes; molecular engines; magnetic field-controlled molecular alignment; dipolar rotors in circularly polarized electric field; ab-initio calculations; solvent effectsMagnetostaticsMolecular physicsSymmetry (physics)Magnetic fieldDipolechemistry.chemical_compoundMagnetic anisotropyNuclear magnetic resonanceElectric fieldPerpendicularGeneral Materials SciencePhysical and Theoretical ChemistryCyclophane
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Spectral investigation of spin echo emission

1993

Abstract The spectral content of the echo radiation emitted after a two-pulse sequence is measured in a two-level spin system. The spectral profiles exhibit maxima and zeroes of spectral density depending on the exciting sequence parameters. A calculation based on a vectorial model relates the zeroes to those packets that happen to be transparent to the second (refocusing) pulse. Moreover we report on a new spectral narrowing effect which we tentatively ascribe to the instantaneous diffusion.

ChemistrySpectral densityPulse sequenceGeneral ChemistryRadiationCondensed Matter PhysicsComputational physicsPulse (physics)Nuclear magnetic resonanceSpectral envelopeMaterials ChemistrySpin echoDiffusion (business)MaximaSolid State Communications
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Determination of the Relative Stereochemistry of Flexible Organic Compounds by Ab Initio Methods: Conformational Analysis and Boltzmann-Averaged GIAO…

2002

Ab initio calculations at the Hartree-Fock level with full-geometry optimization using the 6-31G(d) basis set, and GIAO (gauge including atomic orbitals) 1 3 C NMR chemical shifts, are presented here as a support in the study of the stereochemistry of low-polar organic compounds having an openchain structure. Four linear stereoisomers, fragments of a natural product previously characterized by experimental 1 3 C NMR spectra, which possesses three stereogenic centers, 11 carbon atoms, and 38 atoms in total, were considered. Conformational searches, by empirical force-field molecular dynamics, pointed out the existence of 8-13 relevant conformers per stereoisomer. Thermochemical calculations …

ChemistryStereochemistryChemical shiftOrganic ChemistryAb initioGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRCatalysisAb initio quantum chemistry methodsComputational chemistryAtomConformational isomerismBasis setChemistry - A European Journal
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Tautomerism and the Protonation/Deprotonation of Isocytosine in Liquid- and Solid-States Studied by NMR Spectroscopy and Theoretical Calculations

2011

Isocytosine crystallizes as a 1:1 ratio of two tautomers in a manner similar to that of the guanine and cytosine pairs in DNA. The solid-state NMR chemical shifts of crystalline neutral isocytosine, the sodium salt of isocytosine, and those of isocytosine hydrochloride were measured and related to the NMR parameters in aqueous and organic solutions. The experimental chemical shifts were compared with those calculated by three different methods: (1) calculations on isolated molecules, (2) calculations on isocytosine clusters of various sizes, and (3) infinite crystal calculations, that is, the gauge-including projector-augmented wave (GIPAW) method. The data obtained with the GIPAW method we…

ChemistryStereochemistryChemical shiftOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyCrystal structureTautomerchemistry.chemical_compoundDeprotonationMoleculePhysical chemistryIsocytosinePhysical and Theoretical Chemistryta116European Journal of Organic Chemistry
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1H,13C and17O NMR study of aromatic ring-substituted monochloro- and monobromo-(E)-3-phenylpropenals

1991

Trans-Cinnamaldehydes (CAs) or o-, m- and p-X-(E)-3-phenylpropenals; (X = Cl or Br) were synthesized and their 1H, 13C and 17O NMR spectra were measured, assigned and analysed. The long-range benzylic couplings are discussed in terms of the conformational characteristics of the related styrene systems. The 1H, 13C and 17O NMR substituent chemical shifts of the CA derivatives were compared with those of styrene and explained by the π-electron delocalization in the conjugated CCCO bond system of CA.

ChemistryStereochemistryChemical shiftSubstituentGeneral ChemistryNuclear magnetic resonance spectroscopyConjugated systemRing (chemistry)Medicinal chemistryStyrenechemistry.chemical_compoundDelocalized electronGeneral Materials ScienceSolvent effectsMagnetic Resonance in Chemistry
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Antivirale Wirkstoffe, 27. Mitt. Die Aminomethinylierung von 5-Oxo-2-pyrazolin-3-carbonsäurederivaten

1986

Aus der mit s-Triazin (1) durchgefuhrten Aminomethinylierung der 5-Oxo-2-pyrazolin-3-carbonsaurederivate 2a,b gehen die 4-Aminomethylen-5-oxo-2-pyrazolin-3-carbonsaurederivat 4a,b und die C-Rubazonsauren 5a,b hervor. Bei 4a deuten die spektroskopischen Daten auf das Vorliegen der Z-Form (Abb. 1), fur 5a auf das der Z-s-cis-(OH)-Form (Abb. 2) hin. Die Strukturtypen 4 und 5 weisen Vertreter mit antiviraler, entzundungshemmender, temperatursenkender und antimykotischer Wirkung auf. Antiviral Agents, XXVII: Aminomethynylation of 5-Oxo-2-pyrazoline-3-carboxylic Acid Derivatives Aminomethynylation of the 5-oxo-2-pyrazoline-3-carboxylic acid derivatives 2a,b by means of s-triazine (1) yields the 4…

ChemistryStereochemistryDrug DiscoveryMass spectrumPharmaceutical ScienceBiological activityNuclear magnetic resonance spectroscopyArchiv der Pharmazie
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Syntheses, Structures and Reactivity of New Intramolecularly Coordinated Tin Alkoxides Based on an Enantiopure Ephedrine Derivative

2011

The syntheses of the tin compounds [LSn]2 (2), spiro-L2Sn (3), [LSnW(CO)5]2 (4), [LSnBr2]2 (5), spiro-L2Sn·SnBr4 (6) and LSn[OC(O)Ph]2 (8), where L = MeN(CH2CMe2O)[(S)-CH(Me)-(R)-CH(Ph)O], and (Ph4P)2SnBr6 (7) are reported. The compounds were characterized by elemental analysis, multinuclear NMR spectroscopy including 119Sn cross polarisation–magic angle spinning NMR (CP–MAS) (2, 3–6), electrospray ionization mass spectrometry (2–4) and single crystal X-ray diffraction analysis (2, 2·C7H8, 3a, 3b, 4·C7H8, 5, 6·C7H8, 7).

ChemistryStereochemistryElectrospray ionizationchemistry.chemical_elementNuclear magnetic resonance spectroscopyMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundEnantiopure drugElemental analysisReactivity (chemistry)TinSingle crystalDerivative (chemistry)European Journal of Inorganic Chemistry
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