Search results for " Relaxation"

showing 10 items of 370 documents

13C NMR spectroscopy of four tertiary methyl norbornenols and norbornanols

1975

Carbon chemical shifts and direct 13C1H coupling constants of 2-endo-methyl-5-norbornen-2-exo-ol, 2-exo-methyl-5-norbornen-2-endo-ol, 2-endo-methylnorbornan-2-exo-ol and 2-exo-methylnorbornan-2-endo-ol have been measured from single samples using a dual probe pulse Fourier transform method.

Coupling constantCarbon-13 NMR satelliteChemistryChemical shiftAnalytical chemistrychemistry.chemical_elementGeneral ChemistryFluorine-19 NMRsymbols.namesakeFourier transform13c nmr spectroscopysymbolsGeneral Materials ScienceTransverse relaxation-optimized spectroscopyCarbonOrganic Magnetic Resonance
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HP-Xe to go: Storage and Transportation of Hyperpolarized 129-Xe

2016

Abstract Recently the spin–lattice relaxation time T 1 of hyperpolarized (HP)- 129 Xe was significantly improved by using uncoated and Rb-free storage vessels of GE180 glass. For these cells, a simple procedure was established to obtain reproducible wall relaxation times of about 18 h. Then the limiting relaxation mechanism in pure Xe is due to the coupling between the nuclear spins and the angular momentum of the Xe–Xe van-der-Waals-molecules. This mechanism can be significantly reduced by using different buffer gases of which CO 2 was discovered to be the most efficient so far. From these values, it was estimated that for a 1:1 mixture of HP-Xe with CO 2 a longitudinal relaxation time of …

CouplingNuclear and High Energy PhysicsAngular momentumSpinsCondensed matter physicsChemistryRelaxation (NMR)BiophysicsAnalytical chemistrychemistry.chemical_element010402 general chemistryCondensed Matter Physics01 natural sciencesBiochemistry0104 chemical sciencessymbols.namesakeXenon0103 physical sciencessymbolsvan der Waals forceTotal pressure010306 general physicsLongitudinal Relaxation Time
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The relaxant effects of cromakalim (BRL 34915) on human isolated airway smooth muscle

1992

Cromakalim (BRL 34915) is a potassium channel opener with therapeutic potential as a bronchodilator in asthma. Cromakalim (0.1–30 μmol/l) inhibited the spontaneous tone of human isolated bronchi n a concentration-related manner being nearly as effective as isoprenaline or theophylline. The order of relaxant potencies (expressed as -log10 IC50 mol/l; mean ±SEM) was isoprenaline (7.29 ± 0.27; n = 8) > cromakalim (5.89 ± 0.12; n = 7) > theophylline (4.07 ±0.13; n = 10). In human bronchi where tone had been raised by addition of histamine (0.1 mmol/l), acetylcholine (0.1 mmol/l) or leukotriene D4 (LTD4, 0.1 μmol/l), the relaxant effect of cromakalim was substantially reduced. Cromakalim suppres…

CromakalimMuscle RelaxationBronchiPharmacologyGlibenclamidechemistry.chemical_compoundTheophyllineIsoprenalinemedicineHumansBenzopyransDrug InteractionsPyrrolesPharmacologyTetraethylammoniumIsoproterenolMuscle SmoothGeneral MedicineAcetylcholineBronchodilator AgentschemistryAnesthesiaSRS-APotassium channel openermedicine.symptomCromakalimHistamineAcetylcholineHistamineMuscle contractionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Effects of SCA40 on human isolated bronchus and human polymorphonuclear leukocytes: comparison with rolipram, SKF94120 and levcromakalim

1996

1. SCA40 (0.1 nM-0.1 mM) produced concentration-dependent suppression of the spontaneous tone of human isolated bronchus (-log EC50 = 6.85 +/- 0.09; n = 10) and reached a maximal relaxation similar to that of theophylline (3 mM). The potency (-log EC50 values) of SCA40 compared to other relaxants was rolipram (7.44 +/- 0.12; n = 9) > SCA40 > or = levcromakalim (6.49 +/- 0.04; n = 6) > SKF94120 (5.87 +/- 0.10; n = 9). 2. When tested against the activity of the isoenzymes of cyclic nucleotide phosphodiesterase (PDE) isolated from human bronchus, SCA40 proved highly potent against PDE III (-log IC50 = 6.47 +/- 0.16; n = 4). It was markedly less potent against PDE IV (4.82 +/- 0.18; n = 4) and …

Cromakalimmedicine.medical_specialtyCardiotonic AgentsNeutrophilsLeukotriene B4Muscle Relaxationchemistry.chemical_elementBronchiIn Vitro TechniquesCalciumPharmacologyLeukotriene B4chemistry.chemical_compound3'5'-Cyclic-GMP PhosphodiesterasesSuperoxidesInternal medicinemedicineHumansBenzopyransPyrrolesRolipramCyclic Nucleotide Phosphodiesterases Type 5PharmacologyCyclic nucleotide phosphodiesterasePhosphoric Diester HydrolasesSuperoxideAnti-Inflammatory Agents Non-SteroidalElastaseImidazolesN-Formylmethionine leucyl-phenylalanineCyclic Nucleotide Phosphodiesterases Type 3PyrrolidinonesBronchodilator AgentsCyclic Nucleotide Phosphodiesterases Type 4N-Formylmethionine Leucyl-PhenylalanineEndocrinologychemistry3'5'-Cyclic-AMP PhosphodiesterasesPyrazinesCalciumLeukocyte ElastaseRolipramCromakalimResearch Articlemedicine.drugBritish Journal of Pharmacology
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DSC, Dilatometric, Dielectric, and1H NMR Studies of Phase Transitions and Molecular Motions in [N(C2H5)4]3M2Cl9 (M = Sb, Bi) Crystals

1995

Results in the dependence of stoichiometry of obtained tetraethylammonium (TEA) chloroantiomonate and chlorobismuthate salts on the molar ratio of reactants used in the synthesis are presented. Seven tetraethylammonium salts are obtained: (TEA) 6 M 8 Cl 30 , TEAMCI 4 , (TEA) 3 M 2 Cl 9 (M = Sb, Bi) and (TEA) 2 SbCl 5 . Preliminary X-ray diffraction studies on (TEA) 3 M 2 Cl 9 (M = Sb, Bi) show that they are isomorphous, crystallizing at room temperature in monoclinic symmetry. The dilatometric, dielectric, and DSC studies show that (TEA) 3 Bi 2 Cl 9 undergoes two phase transitions at T c2 = 144 K and at T c1 = 322 K while (TEA) 3 Sb 2 Cl 9 undergoes three transitions at T c3 = 185, T c2 = 2…

CrystalCrystallographyPhase transitionFerroelasticityChemistryStereochemistryProton NMRSpin–lattice relaxationDielectricAtmospheric temperature rangeCondensed Matter PhysicsStoichiometryElectronic Optical and Magnetic Materialsphysica status solidi (b)
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Statics and Dynamics of a Glassy Crystal: A NMR- and Neutron Scattering Investigation of (NaCl) 0.35 (NaCN) 0.65

1987

The statics and the dynamics of the glass transition in (NaCl)0.35(NaCN)0.65 have been investigated by inelastic neutron scattering and are directly compared to NMR results. Insight into the relaxation dynamics is gained via the temperature dependence of the transverse acoustic phonon modes and via the spin relaxation time T1. The statics of the system is reflected by the growth of a central peak and by the distribution of electric-field gradients. Both quantities are directly related to the glass order parameter. The temperature dependence of the order parameter provides experimental evidence that in NaCl:NaCN mixed crystals the glass transition is dominated by random fields rather than by…

CrystalMaterials scienceCondensed matter physicsChemical physicsPhononSpin–lattice relaxationGeneral Physics and AstronomyRelaxation (physics)Inelastic scatteringNeutron scatteringGlass transitionInelastic neutron scatteringEurophysics Letters (EPL)
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The structure and phase transition of mixed crystals

1996

The phase transition and molecular motions of methylammonium cations are studied in the temperature range from 110 to 450 K in the (x = 0.22, 0.345) (MACAB) crystal by x-ray DSC, dilatometric, dielectric and NMR techniques. It is shown that MACAB (x = 0.22) undergoes a structural phase transition at 222 K. The second moment of the NMR line () and the temperature dependence of spin lattice relaxation time () results are interpreted in terms of ( ion dynamics. In the high-temperature phase (I) the cations undergo isotropic reorientations. In the low-temperature phase (II) only one of three cations is still disordered, whereas the two others perform a type of reorientation about their C - N ax…

CrystalPhase transitionCrystallographyChemistryStereochemistryPhase (matter)Spin–lattice relaxationSecond moment of areaGeneral Materials ScienceDielectricAtmospheric temperature rangeCondensed Matter PhysicsIonJournal of Physics: Condensed Matter
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Structure, phase transitions and molecular motions in ferroelastic (C4H8NH2)SbCl6·(C4H8NH2)Cl

2002

The crystal structure at 293 K of the new pyrrolidinium chloroantimonate (V) analogue, (C4H8NH2)SbCl6(C4H8NH2)Cl, has been determined by x-ray diffraction as monoclinic, space group P21/c, Z = 8. The crystal is built up of isolated SbCl6- anions, two types of inequivalent pyrrolidinium cation and isolated Cl- ions. It undergoes five solid-solid phase transitions: at 351/374 K of first-order type (cooling/heating, respectively), at 356 and 152 K second order and at 135/141 and 105/134 K first order, detected by differential scanning calorimetry, dilatometric and dielectric measurements. The ferroelastic domain structure appears between 152 and 135 K. The proton nuclear magnetic resonance sec…

CrystalPhase transitionCrystallographyFerroelasticityDifferential scanning calorimetryChemistryRelaxation (NMR)Spin–lattice relaxationGeneral Materials ScienceCrystal structureCondensed Matter PhysicsMonoclinic crystal systemJournal of Physics: Condensed Matter
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1H NMR, DSC, dielectric, and dilatometric studies of phase transitions and molecular dynamics in N (C2H5)4SbCl4

1994

The results of dielectric, dilatometric, 1H NMR, and DSC studies on N(C2H5)4SbCl4 crystals are presented. The title compound undergoes two phase transitions at Tc1 = 272 K reversible of first order and at Tc2 = 393 K irreversible. The values of transition entropies and enthalpies are compared with those of other tetraethylammonium halogenoantimonates and bismuthates (III). The spin-lattice relaxation times and the values of the second moments of the 1H NMR line for the N(C2H5)4SbCl4 crystal are measured in the temperature range of 70 to 400 K. Two minima of T1 are observed. They are attributed to CH3 group reorientations. The activation energies for the processes are determined.

CrystalPhase transitionNuclear magnetic resonanceChemistryRelaxation (NMR)Spin–lattice relaxationProton NMRPhysical chemistryActivation energyDielectricAtmospheric temperature rangeCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsPhysica Status Solidi (a)
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Solid state NMR studies of gels derived from low molecular mass gelators

2016

The emergence of NMR crystallography provides a unique opportunity to study solids, gels and xerogels, thereby providing ample information to elucidate molecular packing in the native gel. This review details the importance as well as the application of solid state NMR spectroscopy combined with other analytical tools to study gels derived from low molecular mass organo- and hydrogelators.

CrystallographyMagnetic Resonance Spectroscopy010405 organic chemistryChemistrySupramolecular chemistryGeneral ChemistryNuclear magnetic resonance crystallographyNuclear magnetic resonance spectroscopyViscoelastic Substances010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesNMR spectra databaseCondensed Matter::Soft Condensed MatterMolecular WeightCrystallographyChemistrySolid-state nuclear magnetic resonanceGels Solid State NMR Supramolecular NanomaterialsMagic angle spinningAnisotropyTransverse relaxation-optimized spectroscopySpectroscopyGelsSoft Matter
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