Search results for "spin resonance"

showing 10 items of 156 documents

Variability of the Si-O-Si angle in amorphous-SiO2 probed by electron paramagnetic resonance and Raman spectroscopy

2009

We report an experimental investigation by electron paramagnetic resonance (EPR) and Raman spectroscopy on a variety of amorphous silicon dioxide materials. Our study by EPR have permitted us to point out that the splitting of the primary hyperfine doublet of the Eγ′ center shows a relevant sample-to-sample variability, changing from ∼41.8 to ∼42.6 mT in the set of materials we considered. The parallel study by Raman spectroscopy has enabled us to state that this variability is attributable to the different Si-O-Si angle characterizing the matrices of the different materials. © 2009 Elsevier B.V. All rights reserved.

Raman scatteringMaterials Chemistry2506 Metals and AlloysAnalytical chemistryRadiation effectCeramics and CompositeCondensed Matter Physiclaw.inventionsymbols.namesakelawElectron spin resonanceMaterials Chemistryamorphous silica structureCoherent anti-Stokes Raman spectroscopyElectron paramagnetic resonanceHyperfine structureRadiationChemistryElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica SperimentaleSilicaCondensed Matter PhysicsRaman scattering Microwave Radiation effects Magnetic properties Raman spectroscopy Silica Radiation Electron spin resonance DefectsElectronic Optical and Magnetic MaterialsAmorphous solidMolecular geometryRaman spectroscopyCeramics and CompositessymbolsMagnetic propertieDefectRaman spectroscopyMicrowaveRaman scatteringMicrowave
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Structural properties of the range-II- and range-III order in amorphous-SiO2 probed by electron paramagnetic resonance and Raman spectroscopy

2010

In the present work we report an experimental investigation by electron paramagnetic resonance spectroscopy on the hyperfine structure of the E. point defect, probing the local arrangement of the network (range-II order), and by Raman spectroscopy on the D 1 and D 2 lines, probing mean features of the network (range-III order). Our studies, performed on a-SiO 2 samples thermally treated at 1000 °C in air for different time durations, show that changes of the hyperfine structure and of the D 1 and D 2 lines occur in a correlated way. These results give strong evidence that the range-II and range-III order properties are intimately related to each other and that these properties are determine…

Raman scatteringMaterials scienceSolid-state physicsAnalytical chemistryParamagnetic materiallaw.inventionPoint defectsymbols.namesakeNuclear magnetic resonancelawElectron spin resonance spectroscopyElectron paramagnetic resonanceHyperfine structureParamagnetic resonanceExperimental investigationSettore FIS/01 - Fisica SperimentaleElectron resonanceSilicon compoundCondensed Matter PhysicsCrystallographic defectElectronic Optical and Magnetic MaterialsAmorphous solidMolecular geometryRaman spectroscopysymbolsHyperfine structureElectron paramagnetic resonanceTime durationRaman spectroscopyRaman scatteringElectron paramagnetic resonance spectroscopySilica difetti di punto proprieta' struturali
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ESR study of the liposome membrane physical parameters in the heating-cooling cycles.

1998

Abstract Changes of dynamic and structural parameters of egg yolk lecithin (EYL) liposome mem­branes in the heating-cooling cycles have been studied using the E S R spin probe method. The investigations were conducted in the range of temperatures from -18 °C to +60 °C. It has been found that in the range of temperatures -15 °C to +45 °C in both the heating and the cooling run the spectroscopic parameters changed practically along the same curve (re­versible changes). However, after exceeding this range of temperatures one of the parameters (partition coefficient of the spin probe 2,2,6,6 -tetramethylpiperidine -1-oxyl; TEMPO) changed along a closed curve, showing the phenomenon of thermal h…

Range (particle radiation)Liposomefood.ingredientMaterials scienceHot TemperatureAnalytical chemistryElectron Spin Resonance SpectroscopyActive surfaceLecithinEgg YolkGeneral Biochemistry Genetics and Molecular BiologySpin probePartition coefficientCold TemperatureCyclic N-OxidesfoodMembraneLiposomesPhosphatidylcholinesMoleculeThermodynamicsSpin LabelsZeitschrift fur Naturforschung. C, Journal of biosciences
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Testing and linearity calibration of films of phenol compounds exposed to thermal neutron field for EPR dosimetry

2015

This paper reports the preliminary results obtained by Electron Paramagnetic Resonance (EPR) measurements on films of IRGANOX® 1076 phenols with and without low content (5% by weight) of gadolinium oxide (Gd2O3) exposed in the thermal column of the Triga Mark II reactor of LENA (Laboratorio Energia Nucleare Applicata) of Pavia (Italy). Thanks to their size, the phenolic films here presented are good devices for the dosimetry of beams with high dose gradient and which require accurate knowledge of the precise dose delivered. The dependence of EPR signal as function of neutron dose was investigated in the fluence range between 10(11) cm(-2) and 10(14) cm(-2). Linearity of EPR response was fou…

Settore ING-IND/20 - Misure E Strumentazione NucleariAnalytical chemistryGadoliniumFluenceTRIGAlaw.inventionNCT dosimetrychemistry.chemical_compoundPhenolslawCalibrationPhenolDosimetryIrradiationElectron paramagnetic resonanceNeutron beamNeutronsRadiationPhenolSettore ING-IND/18 - Fisica Dei Reattori NucleariSettore FIS/01 - Fisica SperimentaleElectron Spin Resonance SpectroscopyNeutron temperatureSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Electron Paramagnetic ResonancechemistryCalibrationNuclear chemistry
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Metal complexes of the carbonic anhydrase inhibitor methazolamide (Hmacm). Crystal structure of the Zn(macm)2 (NH3)2. Anticonvulsant properties of th…

1995

Complexes of Co(II), Cu(II), and Zn(II) with deprotonated methazolamide and ammonia are synthesized and characterized. The complex Zn(macm)2(NH3)2 crystallizes in the monoclinic C2/c space group with a = 13.468(1), b = 6.759(1), c = 23.014(2) A, beta = 90.27(1), and Z = 4. The structure was refined to R = 0.049 (Rw = 0.053). The Zn(II) ion is coordinated to two deprotonated sulfonamido nitrogen atoms of the macm- ligand and two nitrogen atoms of the ammonia ligands in a distorted tetrahedron. The Zn(macm)2(NH3)2 complex is shown to be a simple model for the methazolamide inhibition of CA. EHMO calculations applied to fractional coordinates of the Zn(macm)2(NH3)2 complex indicate that the at…

Spectrophotometry InfraredCations DivalentInorganic chemistryMethazolamidechemistry.chemical_elementCrystal structureZincCrystallography X-RayBiochemistryInorganic ChemistryMetalDeprotonationmedicineAnimalsMethazolamideHOMO/LUMOMolecular StructureChemistryLigandElectron Spin Resonance SpectroscopyCobaltZincCrystallographyvisual_artvisual_art.visual_art_mediumAnticonvulsantsCoppermedicine.drugMonoclinic crystal systemJournal of Inorganic Biochemistry
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Synthesis, characterization, and crystal structure of [Cu(cinoxacinate)2] · 2H2O complex: A square-planar CuO4 chromophore. Antibacterial studies

1995

The structural and spectroscopic properties of a new copper (II) complex of cinoxacin (HCx) have been investigated. The complex [Cu(Cx)2].2H2O crystallizes in the monoclinic system, space group P2(1)/c. The cell dimensions are: a = 7.998(2), b = 7.622(1), c = 18.955(6) A, beta = 94.38(2) degree, V = 1154.6(6) A3, Z = 2. The structure was refined to R = 0.051. The crystal is composed of [Cu(Cx)2] units and uncoordinated water molecules. The Cu(II) ion, at a center of symmetry, is coordinated to two cinoxacinate (Cx) ligands related by the inversion center. Each cinoxacinate acts as bidentate ligand bonded to the cation through its carboxylate oxygen atom and through its exocyclic carbonyl ox…

Spectrophotometry InfraredStereochemistryCrystal structureMicrobial Sensitivity TestsCrystallography X-RayBiochemistryInorganic ChemistryCrystalchemistry.chemical_compoundEnterobacteriaceaeOrganometallic CompoundsMoleculeCarboxylateGroup 2 organometallic chemistryGram-Negative Aerobic BacteriaMolecular StructureChemistryLigandSpectrophotometry AtomicElectron Spin Resonance SpectroscopyChromophoreGram-Positive CocciSolubilityCinoxacinSpectrophotometry UltravioletCopperMonoclinic crystal system
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Influence of neutron and gamma-ray irradiations on rad-hard optical fiber

2015

We investigated point defects induced in rad-hard Fluorine-doped optical fibers using both a mixed source of neutrons (fluences from 1015 to 1017 n/cm2) and γ-rays (doses from 0.02 to 2 MGy) and by a γ-ray source (dose up to 10 MGy). By combining several complementary spectroscopic techniques such as radiation-induced attenuation, confocal micro-luminescence, time-resolved photo-luminescence and electron paramagnetic resonance, we evidenced intrinsic and hydrogen-related defects. The comparison between the two irradiation sources highlights close similarities among the spectroscopic properties of the induced defects and the linear correlation of their concentration up to 1016 n/cm2. These r…

Spectroscopy Fluorescence and luminescenceRadiationPhotoluminescenceMaterials sciencebusiness.industryAstrophysics::High Energy Astrophysical PhenomenaGamma rayFiber opticRadiationElectron spin resonance.Crystallographic defectMolecular physicsAbsorptionElectronic Optical and Magnetic Materialslaw.inventionlawNeutron flux[SPI.OPTI]Engineering Sciences [physics]/Optics / PhotonicOptoelectronicsNeutronDefectIrradiationbusinessElectron paramagnetic resonanceOptical Materials Express
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Ascorbic Acid Oxidation in Sucrose Aqueous Model Systems at Subzero Temperatures

2004

The reduction of Tempol by ascorbic acid in concentrated sucrose solutions was measured by electron paramagnetic resonance (EPR) at temperatures ranging from 16 to −16 °C. This method allowed the determination of the rate constants (k) of this fast reaction, by recording the Tempol reduction as a function of time. The two reactants were initially separated and had to migrate for the reaction to occur. The experimental findings were compared with predicted values according to the equation for diffusion-controlled reaction proposed by Atkins. The experimental reaction rate constants were observed to be lower than the calculated ones. However, the experimental values were found to be controlle…

SucroseSucroseReactionDiffusionAnalytical chemistryAscorbic Acid010402 general chemistry01 natural scienceslaw.inventionCyclic N-OxidesReaction rate[SPI]Engineering Sciences [physics]chemistry.chemical_compoundViscosityReaction rate constantlawFreezing0103 physical sciencesVitamin CElectron paramagnetic resonanceAqueous solution010304 chemical physicsdiffusionElectron Spin Resonance SpectroscopyTemperatureWaterTempolNegative temperaturesGeneral ChemistryAscorbic acid0104 chemical sciencesSolutionsKineticschemistryBiochemistrySpin LabelsElectron paramagnetic resonanceGeneral Agricultural and Biological SciencesOxidation-ReductionCryoconcentrationJournal of Agricultural and Food Chemistry
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DNA cleavage reaction induced by dimeric copper(II) complexes of N-substituted thiazole sulfonamides

2005

A new dinuclear copper(II) complex has been synthesised and structurally characterised: [Cu2(tz-ben)4] (Htz-ben = N-thiazol-2-yl-benzenesulfonamide). Its crystal structure, magnetic properties and electronic paramagnetic resonance (EPR) spectra were studied in detail. In the compound the metal centres are bridged by four non-linear triatomic NCN groups. The coordination geometry of the copper ions in the dinuclear entity is distorted square pyramidal (4+1). Two thiazole N and two sulfonamido N atoms occupy the equatorial positions and one sulfonamido O atom is in the axial position. Magnetic susceptibility data show a strong antiferromagnetic coupling, -2J = 114.1 cm(-1). The EPR spectra of…

SulfonamidesSpectrophotometry InfraredStereochemistryElectron Spin Resonance SpectroscopyDNACrystal structureZero field splittingCrystallography X-RayBiochemistryMagnetic susceptibilityMass SpectrometrySquare pyramidal molecular geometrylaw.inventionInorganic ChemistryThiazolesCrystallographychemistry.chemical_compoundchemistrylawOrganometallic CompoundsSinglet stateThiazoleElectron paramagnetic resonanceCopperCoordination geometryJournal of Inorganic Biochemistry
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Reinforced Room-Temperature Spin Filtering in Chiral Paramagnetic Metallopeptides

2020

Chirality-induced spin selectivity (CISS), whereby helical molecules polarize the spin of electrical current, is an intriguing effect with potential applications in nanospintronics. In this nascent field, the study of the CISS effect using paramagnetic chiral molecules, which could introduce another degree of freedom in controlling the spin transport, remains so far unexplored. To address this challenge, herein we propose the use of self-assembled monolayers (SAMs) of helical lanthanide-binding peptides. To elucidate the effect of the paramagnetic nuclei, monolayers of the peptide coordinating paramagnetic or diamagnetic ions are prepared. By means of spin-dependent electrochemistry, the CI…

Surface PropertiesFOS: Physical sciencesApplied Physics (physics.app-ph)02 engineering and technology010402 general chemistryLanthanoid Series Elements01 natural sciencesBiochemistryCatalysisElectron TransportParamagnetismColloid and Surface ChemistryElectrical currentMesoscale and Nanoscale Physics (cond-mat.mes-hall)ElectrochemistryOrganometallic CompoundsMoleculeAmino Acid SequenceSpin-½Spin filteringCondensed Matter - Mesoscale and Nanoscale PhysicsCondensed matter physicsChemistryElectron Spin Resonance SpectroscopyTemperatureStereoisomerismPhysics - Applied PhysicsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesModels ChemicalCondensed Matter::Strongly Correlated ElectronsGoldPeptides0210 nano-technologySelectivityJournal of the American Chemical Society
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