Search results for "Spin–lattice relaxation"

showing 10 items of 50 documents

NMR T1-Relaxation Measurements on Paramagnetic Organolanthanides: An Alternative Tool for Structure Determination in Solution

2005

1H NMR investigations were conducted on four paramagnetic organolanthanides, all bearing the tetraisopropylcyclopentadienyl ligand Cp4i (HC5iPr4) in order to verify whether or not interactions observed in the solid state are maintained in solution. In some cases variable-temperature experiments were necessary to enhance the resolution and determine the best conditions for the study. The 1D NMR spectrum could be interpreted in every case. Complementary 2D COSY experiments allowed the full attribution of the signals. T1 (1H) relaxation values were determined for all the paramagnetic complexes at the most suitable temperature, and compared with those of the diamagnetic KCp4i. The same tendency…

010405 organic chemistryChemistryLigandRelaxation (NMR)Analytical chemistrySpin–lattice relaxation[ CHIM.COOR ] Chemical Sciences/Coordination chemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesParamagnetic complexesInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographyNMR spectroscopyOxidation stateLanthanidesProton NMR[CHIM.COOR]Chemical Sciences/Coordination chemistryMethyl groupSpin-lattice relaxation times
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Reorientations and translations in a fragile glass-former: magnetic resonance studies of meta-fluoroaniline

1999

Abstract The rotational dynamics in supercooled liquid and glassy meta-fluoroaniline was studied using proton and fluorine spin-lattice relaxation times. It is shown that while proton relaxation is dominated by homonuclear relaxation, for fluorine heteronuclear relaxation prevails. The results could be well described using a distribution of correlation times. The mean correlation times show pronounced deviations from the simple Arrhenius law. In addition translational self-diffusion coefficients were measured for T>200 K using a static magnetic field gradient technique.

Arrhenius equationCondensed matter physicsProtonChemistryOrganic ChemistrySpin–lattice relaxationMagnetostaticsHomonuclear moleculeAnalytical ChemistryInorganic ChemistrySpin–spin relaxationsymbols.namesakeHeteronuclear moleculesymbolsRelaxation (physics)SpectroscopyJournal of Molecular Structure
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Self-trapped exciton luminescence in crystalline α-quartz under two-photon laser excitation

2003

Abstract The luminescence of pure crystalline α-quartz is studied under pulsed ArF laser excitation. The luminescence parameters obtained correspond well with those of self-trapped excitons (STEs) in α-quartz, indicating that the excitation process is two-photon. The efficiency of two-photon excitation is of the same order of magnitude as the one-photon excitation of sodium salicylate. The STE luminescence decay kinetics and their temperature dependence under photoexcitation were recorded with higher accuracy than previously. Changes in the decay kinetics with temperature are explained by the splitting of the STE triplet state in zero magnetic field and are analyzed with the assumption of t…

ChemistryExcitonRelaxation (NMR)Spin–lattice relaxationPhysics::OpticsGeneral ChemistryCondensed Matter PhysicsPhotoexcitationCondensed Matter::Materials ScienceTwo-photon excitation microscopyPhysics::Atomic and Molecular ClustersMaterials ChemistryTriplet stateAtomic physicsLuminescenceExcitationSolid State Communications
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Low-temperature methyl group dynamics of hexamethylbenzene in crystalline and glassy matrices as studied by 2H NMR

1991

Abstract 2 H NMR spectra of hexamethylbenzene (HMB) in protonated crystalline and amorphous matrices at low temperatures are presented. All spectra reveal lineshape changes which can be attributed to methyl group tunnelling. Compared to neat HMB, a drastic increase of the tunnelling frequency is found for all systems. This indicates that the hindering potential originates predominantly from intermolecular forces. We studied the temperature dependence of these spectra and the spin-lattice relaxation in order to exclude a distribution of motional correlation times describing a thermally activated process. In addition, we find a distortion of the methyl tetrahedron.

ChemistryIntermolecular forceRelaxation (NMR)Spin–lattice relaxationGeneral Physics and AstronomyNuclear magnetic resonance spectroscopyAmorphous solidchemistry.chemical_compoundNuclear magnetic resonanceProton NMRHexamethylbenzenePhysical chemistryPhysical and Theoretical ChemistryMethyl groupChemical Physics Letters
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Phase transition kinetics and reorientational dynamics of the plastic crystal meta-carborane studied by deuteron NMR

2002

Meta-carborane shows an orientationally disordered, orthorhombic phase which transforms into an ordered monoclinic phase near 170 K and into a quasi-isotropic cubic phase near 280 K. From deuteron magnetization measurements both transitions are found to exhibit a thermal hysteresis and slow transformation kinetics. Furthermore, solid-echo NMR spectra and spin-lattice relaxation times are reported. These results indicate that in the orthorhombic phase the meta-carborane molecules perform a strongly anisotropic motion which is characterized by a temperature dependent amplitude.

ChemistryRelaxation (NMR)Spin–lattice relaxationThermodynamicsCondensed Matter Physics530Electronic Optical and Magnetic MaterialsNMR spectra databaseMagnetizationCrystallographyCondensed Matter::Materials SciencePhase (matter)Materials ChemistryCeramics and CompositesOrthorhombic crystal systemCondensed Matter::Strongly Correlated ElectronsPlastic crystalMonoclinic crystal system
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Crystal structure, dielectric properties and molecular motions in ( i -C 4 H 9 NH 3 ) 3 Bi 2 Br 9

2000

Abstract The crystal structure of ( i -C 4 H 9 NH 3 ) 3 Bi 2 Br 9 at room temperature has been determined and refined to R =0.036. The crystal is orthorhombic, space group Ama 2. The structure is built up of the i -butylammonium cations and isolated Bi 2 Br 9 3− anions. The complex dielectric permittivity along the a -axis has been measured between 500 Hz and 1000 MHz in the vicinity of two phase transitions at 252 and 263 K. The dielectric response close to 252 K is well described by the Debye equation. The activation energy of the reorientation of the i -butylammonium cations is found to be 0.68 eV. The temperature dependencies of the proton relaxation time T 1 and of the second moment of…

ChemistryStereochemistryRelaxation (NMR)Spin–lattice relaxationGeneral ChemistryCrystal structureActivation energyDielectricCondensed Matter PhysicsCrystalCrystallographyProton NMRGeneral Materials ScienceOrthorhombic crystal systemJournal of Physics and Chemistry of Solids
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Nonexponential 2H spin-lattice relaxation as a signature of the glassy state

1990

Abstract High-precision measurements of 2H spin-lattice relaxation on several molecular glass-forming liquids have been performed. As a general feature the following can be stated: At temperatures more than ten to twenty degrees above the calorimetric glass transition temperature Tg the 2H spin-lattice relaxation is exponential; below that temperature regime the relaxation is nonexponential. This crossover from exponential to nonexponential magnetization recovery implies that no common spin temperature caused by spin diffusion exists in a 2H glass. This contrasts 1H spin-lattice relaxation which is found to be strictly monoexponential throughout. The occurrence of nonexponential 2H relaxati…

Condensed matter physicsChemistrySpin–lattice relaxationGeneral Physics and AstronomyObservableCondensed Matter::Disordered Systems and Neural NetworksExponential functionMagnetizationNuclear magnetic resonanceSpin diffusionRelaxation (physics)Physical and Theoretical ChemistryGlass transitionSpin-½Chemical Physics Letters
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β-process of supercooled o-terphenyl: a comparison of dielectrical and NMR data guided by mode-coupling theory

1990

Abstract According to predictions of mode-coupling theory of the liquid-glass transition, a Cole-Cole dynamical susceptibility is applied to the β-relaxation of supercooled o -terphenyl as studied by 2 H NMR spin-lattice relaxation and by dielectrical relaxation. A temperature-dependent amplitude (1- f ) is assumed for the β-process which yields a description of the NMR data consistent with the dielectrical data. The plateau value f separating the α- and β-processes in the two-step correlation function reveals a similar temperature dependence as compared to the Debye-Waller factor.

Condensed matter physicsRelaxation (NMR)Spin–lattice relaxationGeneral Physics and AstronomyThermodynamicsNuclear magnetic resonance spectroscopychemistry.chemical_compoundMolecular dynamicsCorrelation functionchemistryTerphenylProton NMRPhysical and Theoretical ChemistrySupercoolingChemical Physics Letters
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Aging in a free-energy landscape model for glassy relaxation. II. Fluctuation-dissipation relations.

2006

Several fluctuation-dissipation relations are investigated for a simple free-energy landscape model designed to describe the primary relaxation in supercooled liquids. The calculations of the response and of the correlation functions are performed for a quench from a high temperature to a low temperature. In the model, all dynamical quantities reach equilibrium after long times, but for times shorter than the re-equilibration time they do not exhibit time-translational invariance and the fluctuation-dissipation theorem is violated. Two measures for these violations are considered. One such measure is given by the slope in a plot of the integrated response versus the correlation function and…

Correlation function (statistical mechanics)ChemistrySpin–lattice relaxationGeneral Physics and AstronomyEnergy landscapeRelaxation (physics)Dielectric lossStatistical physicsPhysical and Theoretical ChemistryDissipationSupercoolingMeasure (mathematics)The Journal of chemical physics
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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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