Search results for "Paramagnetic"

showing 10 items of 600 documents

Trapping a Highly Reactive Nonheme Iron Intermediate That Oxygenates Strong C—H Bonds with Stereoretention

2015

An unprecedentedly reactive iron species (2) has been generated by reaction of excess peracetic acid with a mononuclear iron complex [FeII(CF3SO3)2(PyNMe3)] (1) at cryogenic temperatures, and characterized spectroscopically. Compound 2 is kinetically competent for breaking strong C-H bonds of alkanes (BDE ≈ 100 kcal·mol-1) through a hydrogen-atom transfer mechanism, and the transformations proceed with stereoretention and regioselectively, responding to bond strength, as well as to steric and polar effects. Bimolecular reaction rates are at least an order of magnitude faster than those of the most reactive synthetic high-valent nonheme oxoiron species described to date. EPR studies in tande…

Steric effectsStereochemistry010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryChemical reactionCatalysisReaccions químiquesCatalysislaw.inventionIron -- ReactivityReaction rateColloid and Surface ChemistrylawChemical reactionsReactivity (chemistry)Electron paramagnetic resonanceAlkylFerro -- Reactivitatchemistry.chemical_classification010405 organic chemistryLigandGeneral Chemistry0104 chemical scienceschemistryJournal of the American Chemical Society
researchProduct

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
researchProduct

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
researchProduct

2019

Abstract In high sensitivity inductive electron spin resonance spectroscopy, superconducting microwave resonators with large quality factors are employed. While they enhance the sensitivity, they also distort considerably the shape of the applied rectangular microwave control pulses, which limits the degree of control over the spin ensemble. Here, we employ shaped microwave pulses compensating the signal distortion to drive the spins faster than the resonator bandwidth. This translates into a shorter echo, with enhanced signal-to-noise ratio. The shaped pulses are also useful to minimize the dead-time of our spectrometer, which allows to reduce the wait time between successive drive pulses.

SuperconductivityNuclear and High Energy PhysicsMaterials scienceSpectrometerSpinsbusiness.industryBiophysics010402 general chemistryCondensed Matter PhysicsArbitrary waveform generator01 natural sciencesBiochemistry030218 nuclear medicine & medical imaging0104 chemical scienceslaw.invention03 medical and health sciencesResonator0302 clinical medicineOpticslawbusinessElectron paramagnetic resonanceSpectroscopyMicrowaveJournal of Magnetic Resonance
researchProduct

The dynamics of magnetic ordering in a natural hemo-ilmenite solid solution

2007

Geophysical Journal International, 169 (3)

Superparamagnetic clustersHemo-ilmeniteMaterials scienceSolid solutionAnalytical chemistryAtmospheric temperature rangeengineering.materialExchange anisotropyEnvironmental magnetism; Exchange anisotropy; Hemo-ilmenite; Low-temperature magnetism; Solid solution; Superparamagnetic clustersCrystallographyMagnetizationEnvironmental magnetismGeophysicsExchange biasGeochemistry and PetrologyFerrimagnetismengineeringAntiferromagnetismLow-temperature magnetismIlmeniteSolid solutionSuperparamagnetismGeophysical Journal International
researchProduct

Radiation-Induced Stable Radicals in Calcium Phosphates: Results of Multifrequency EPR, EDNMR, ESEEM, and ENDOR Studies

2021

This article presents the results of a study of radiation-induced defects in various synthetic calcium phosphate (CP) powder materials (hydroxyapatite—HA and octacalcium phosphate—OCP) by electron paramagnetic resonance (EPR) spectroscopy at the X, Q, and W-bands (9, 34, 95 GHz for the microwave frequencies, respectively). Currently, CP materials are widely used in orthopedics and dentistry owing to their high biocompatibility and physico-chemical similarity with human hard tissue. It is shown that in addition to the classical EPR techniques, other experimental approaches such as ELDOR-detected NMR (EDNMR), electron spin echo envelope modulation (ESEEM), and electronnuclear double resonance…

TechnologyMaterials scienceQH301-705.5QC1-999Radical02 engineering and technology010402 general chemistry01 natural sciencesRadiation-induced centerSpectral linelaw.inventioncalcium phosphateCrystalEDNMRlawGeneral Materials ScienceBiology (General)Electron paramagnetic resonanceSpectroscopyQD1-999InstrumentationHyperfine structureFluid Flow and Transfer ProcessesTPhysicsProcess Chemistry and TechnologyGeneral EngineeringResonanceENDOREngineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyHyperfine interaction3. Good health0104 chemical sciencesComputer Science Applicationshyperfine interactionChemistryCalcium phosphateQuadrupole:NATURAL SCIENCES [Research Subject Categories]ESEEMPhysical chemistryTA1-20400210 nano-technologyradiation-induced centerApplied Sciences
researchProduct

Oxidation State and Local Structure of Chromium Ions in LaOCl

2021

This research is funded by the Latvian Council of Science, project “Novel transparent nanocomposite oxyfluoride materials for optical applications”, project No. LZP-2018/1-0335. Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017- TeamingPhase2 under grant agreement No. 739508, project CAMART2.

Technologyelectron-nuclear double resonance (ENDOR)Materials sciencechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesArticlelaw.inventionChromiumLattice constantX-ray photoelectron spectroscopyLaOCl; chromium; X-ray photoelectron spectroscopy (XPS); X-ray absorption spectroscopy; electron paramagnetic resonance (EPR); electron-nuclear double resonance (ENDOR)lawOxidation state:NATURAL SCIENCES:Physics [Research Subject Categories]General Materials ScienceElectron paramagnetic resonanceMicroscopyQC120-168.85X-ray absorption spectroscopyTReducing atmosphereQH201-278.5X-ray absorption spectroscopy600X-ray photoelectron spectroscopy (XPS)Engineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyXANESTK1-99710104 chemical sciences3. Good healthLaOClelectron paramagnetic resonance (EPR)Descriptive and experimental mechanicschemistry13. Climate actionPhysical chemistryElectrical engineering. Electronics. Nuclear engineeringchromiumTA1-20400210 nano-technologyddc:600Materials
researchProduct

Synthesis, crystal structure, spectroscopic characterisation and magnetic properties of [Cu2(BIBM)2(C2O4)2]·4H2O (BIBM=bis(2-imidazolyl)bis(methoxyca…

2001

Abstract The structure and spectroscopic and magnetic properties of bis(μ-1,2,3-oxalato)bis[bis(2-imidazolyl)bis(methoxycarbonyl)methylmethane]dicopper(II) tetrahydrate are described. The compound is built of centrosymmetric neutral dimeric [Cu2(BIBM)2(C2O4)2] entities linked through hydrogen bonds involving water molecules and oxalate groups. In the dimeric unit the two centrosymmetrically related copper — which are involved in CuN2O2O2′ chromophores lying in an elongated octahedral environment — are bridged through the oxalate group which acts in a bidentate–monodentate (μ-1,2,3) fashion. Both electronic and EPR spectra are indicative of an essentially dx2−y2 ground state for the copper(I…

TetrahydrateChemistryHydrogen bondStereochemistryCrystal structureMagnetic susceptibilityOxalatelaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronlawMaterials ChemistryMoleculePhysical and Theoretical ChemistryElectron paramagnetic resonanceInorganica Chimica Acta
researchProduct

Synthesis and magnetic properties of bis(μ-hydroxo)bis[(2,2 ′-bipyridyl)copper(II)] squarate. Crystal structure of bis(μ-hydroxo)bis[(2,2′-bipyridyl)…

1990

Abstract The compound [Cu2(bipy)2(OH)2](C4O4)·5.5H2O, where bipy and C4O42− correspond to 2,2′-bipyridyl and squarate (dianion of 3,4-dihydroxy-3-cyclo- butene-1,3-dione) respectively, has been synthesized. Its magnetic properties have been investigated in the 2–300 K temperature range. The ground state is a spin-triplet state, with a singlet-triplet separation of 145 cm−1. The EPR powder spectrum confirms the nature of the ground state. Well-formed single crystals of the tetrahydrate, [Cu2(bipy)2(OH)2](C4O4)·4H2O, were grown from aqueous solutions and characterized by X-ray diffraction. The system is triclinic, space group P 1 , with a = 9.022(2), b = 9.040(2), c = 8.409(2) A, α = 103.51(2…

TetrahydrateStereochemistrychemistry.chemical_elementCrystal structureTriclinic crystal systemMagnetic susceptibilityCopperlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceHydrateInorganica Chimica Acta
researchProduct

Photo- and Thermochromic and Adsorption Properties of Porous Coordination Polymers Based on Bipyridinium Carboxylate Ligands

2015

The zwitterionic bipyridinium carboxylate ligand 1-(4-carboxyphenyl)-4,4'-bipyridinium (hpc1) in the presence of 1,4-benzenedicarboxylate anions (BDC(2-)) and Zn(2+) ions affords three porous coordination polymers (PCPs): [Zn5(hpc1)2(BDC)4(HCO2)2]·2DMF·EtOH·H2O (1), [Zn3(hpc1)(BDC)2(HCO2)(OH)(H2O)]·DMF·EtOH·H2O (2), and [Zn10(hpc1)4(BDC)7(HCO2)2(OH)4(EtOH)2]·3DMF·3H2O (3), with the formate anions resulting from the in situ decomposition of dimethylformamide (DMF) solvent molecules. 1 and 3 are photo- and thermochromic, turning dark green as a result of the formation of bipyridinium radicals, as shown by electron paramagnetic resonance measurements. Particularly, crystals of 3 are very photo…

Thermochromism010405 organic chemistryLigand010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistrySolventchemistry.chemical_compoundchemistrylawPolymer chemistryDimethylformamideMoleculeOrganic chemistry[CHIM]Chemical SciencesFormateCarboxylatePhysical and Theoretical ChemistryElectron paramagnetic resonanceComputingMilieux_MISCELLANEOUS
researchProduct