Search results for "Paramagnetic"

showing 10 items of 600 documents

UV-Photoinduced Defects In Ge-Doped Optical Fibers

2005

We investigated the effect of continuous-wave (cw) UV laser radiation on single-mode Ge-doped H2- loaded optical fibers. An innovative technique was developed to measure the optical absorption (OA) induced in the samples by irradiation, and to study its dependence from laser fluence. The combined use of the electron spin resonance (ESR) technique allowed the structural identification of several radiation-induced point defects, among which the Ge(1) (GeO4 -) is found to be responsible of induced OA in the investigated spectral region.

Condensed Matter - Materials ScienceMaterials scienceOptical fiberbusiness.industryDopingMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesDisordered Systems and Neural Networks (cond-mat.dis-nn)RadiationCondensed Matter - Disordered Systems and Neural NetworksFluenceCrystallographic defectoptical fibers radiation effects radiation-induced attenuationlaw.inventionlawOptoelectronicsIrradiationAbsorption (electromagnetic radiation)businessElectron paramagnetic resonance
researchProduct

Tuning of the photoinduced charge transfer process in donor-acceptor "double cable" copolymers

2003

The covalent linking of acceptor molecules to electron donating conjugated polymer is an approach for the development of new photoactive materials for the fabrication of organic photoelectric conversion devices. With this strategy we have designed a polyalkylthiophene copolymer series containing in the side chain anthraquinone molecules as electron acceptor. The peculiar features of the copolymers are the good processability and the ease in tailoring the content of acceptor moieties. Their potential use as photoactive materials is investigated in terms of the photoinduced charge transfer properties, studied by FTIR photoinduced absorption and Light Induced Electron Spin Resonance spectrosco…

Condensed Matter PhysicConjugated systemPhotochemistryAnthraquinonePhotoinduced electron transferlaw.inventionchemistry.chemical_compoundlawMaterials ChemistryMoleculeDonor-acceptor alkylthiophene copolymerPhotoinduced charge transferElectron paramagnetic resonanceMechanical EngineeringElectronic Optical and Magnetic MaterialMetals and AlloysSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsAcceptorElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsCovalent bondPolythiopheneLight-induced electron spin resonancePhotoinduced absorption
researchProduct

Trapping of laser-vaporized alkali metal atoms in rare-gas matrices

1999

Abstract Alkali metal atoms prepared by laser ablation of solid Li and Na are trapped in Ar, Kr, and Xe matrices and studied by electron paramagnetic resonance spectroscopy (EPR) at 15 K. Evidence for tight trapping sites, not observed for atoms generated by conventional Knudsen oven techniques, is presented. The novel tight trapping sites are characterized by a large increase in the isotropic hyperfine coupling constant and a simultaneous decrease in the isotropic g -value. Based on the EPR data, it is suggested that the observed tight trapping corresponds to single substitution of lattice atoms in Ar, Kr, and Xe matrices.

Condensed Matter::Quantum GasesLaser ablationChemistryIsotropyGeneral Physics and AstronomyTrappingAlkali metalLaserlaw.inventionlawLattice (order)Physics::Atomic PhysicsKnudsen numberPhysical and Theoretical ChemistryAtomic physicsElectron paramagnetic resonanceChemical Physics Letters
researchProduct

Single-crystal EPR spectroscopy of a Co(II) single-chain magnet

2013

Abstract An electron paramagnetic resonance (EPR) study of a single crystal of Co II -based single-chain magnets (SCM) is presented. Discrete resonant absorptions are associated to the presence of magnetic domains within the chains of finite lengths determined by a competition between intra-chain exchange interactions and thermally excited single spin fluctuations. The results are interpreted as a transition from single spin dynamics at high temperature ( T  ∼20 K), associated to the Kramers doublet ground state of the individual Co II ions, to archetypical SCM dynamics at low temperatures, where intra-chain correlations form long magnetic domains, whose average length is imposed by the con…

Condensed matter physicsMagnetic domainChemistryMolecular physicslaw.inventionIonInorganic ChemistrylawExcited stateMagnetMaterials ChemistryPhysical and Theoretical ChemistryGround stateElectron paramagnetic resonanceSpin (physics)Single crystalPolyhedron
researchProduct

Intramolecular proton transfer boosts water oxidation catalyzed by a Ru complex

2015

We introduce a new family of complexes with the general formula [Run(tda)(py)2]m+ (n = 2, m = 0, 1; n = 3, m = 1, 2+; n = 4, m = 2, 32+), with tda2– being [2,2′:6′,2″-terpyridine]-6,6″-dicarboxylate, including complex [RuIV(OH)(tda-κ-N3O)(py)2]+, 4H+, which we find to be an impressive water oxidation catalyst, formed by hydroxo coordination to 32+ under basic conditions. The complexes are synthesized, isolated, and thoroughly characterized by analytical, spectroscopic (UV–vis, nuclear magnetic resonance, electron paramagnetic resonance), computational, and electrochemical techniques (cyclic voltammetry, differential pulse voltammetry, coulometry), …

Coordination numberInorganic chemistryGeneral ChemistryElectrochemistryBiochemistryCatalysislaw.inventionCrystallographychemistry.chemical_compoundColloid and Surface ChemistryCatalytic oxidationchemistryOxidation statelawDifferential pulse voltammetryCarboxylateCyclic voltammetryElectron paramagnetic resonance
researchProduct

EPR hyperfine structure of F‐type centres in pure LiBaF 3 crystal

2007

We studied EPR spectra of pure LiBaF3 sample of high quality. For EPR measurements LiBaF3 sample was X-irradiated at room temperature, however spectra could be observed at low temperatures - at 77 K. All hyperfine structure lines of F-type centre could be well resolved contrary to our earlier studies of Fe doped LiBaF3 crystal. Qualitative analysis with g-tensor parameters derived from magneto-optical measurements showed that the F-type centre observed earlier by MCD-EPR techniques is the same F-type centre we observe with the EPR. We analyse origin of the hyperfine structure of the EPR spectra and their angular dependencies and discuss the structure of F-type centres in the LiBaF3 crystal.…

CrystalCrystallographyQualitative analysisFe dopedlawChemistryAnalytical chemistryCondensed Matter PhysicsElectron paramagnetic resonanceHyperfine structureSpectral linelaw.inventionphysica status solidi c
researchProduct

Epoxidation of stilbene using supported gold nanoparticles: cumyl peroxyl radical activation at the gold nanoparticle surface.

2014

The catalytic epoxidation of cis-stilbene using cumene as a solvent in the presence of supported gold nanoparticles (AuNP) yields a mixture of cis and trans-stilbene oxides. EPR and product distribution studies support a new mechanistic proposal where oxygen centred radicals activate the AuNP surface and form active surface oxygen species responsible for the epoxidation products.

CumeneChemistryRadicalMetals and AlloysNanoparticleGeneral ChemistryPhotochemistryCatalysisProduct distribution3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCatalysisSolventchemistry.chemical_compoundlawColloidal goldMaterials ChemistryCeramics and CompositesElectron paramagnetic resonanceChemical communications (Cambridge, England)
researchProduct

Copper-Assisted Hemiacetal Synthesis: A Cu II Chain Obtained by a One-Step in situ Reaction of Picolinaldehyde

2014

International audience; The 1D polymer complex [Cu2(L)2(SCN)2]n (1 ) has been synthesised in a one‐step in situ reaction of picolinaldehyde with sodium thiocyanate. The complex 1 was characterised by FTIR spectroscopy, UV/Vis spectrophotometry and elemental analysis. The crystal structure of complex 1 shows that chains of dimer complexes are formed with tetra‐ and pentacoordinate copper centres alternately linked by one thiocyanato and two alkoxido bridges. Variable‐temperature magnetic measurements showed a strong antiferromagnetic interaction between the copper centres within the dimer mediated by the two alkoxido bridges with a J value of –374 cm–1, which is in agreement with the DFT‐cal…

Cyclic voltammetryDimerInorganic chemistrychemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundlawSpectrophotometryMagnetic propertiesmedicine[CHIM]Chemical SciencesElectron paramagnetic resonancePolynuclear complexesmedicine.diagnostic_testCopperIn situ ligand synthesisCrystallographyDensity functional calculationschemistryHemiacetalSodium thiocyanateCyclic voltammetryCopperEPR spectroscopy
researchProduct

Spectroscopic and DFT Characterization of a Highly Reactive Nonheme FeV–Oxo Intermediate

2018

The reaction of [(PyNMe3)FeII(CF3SO3)2], 1, with excess peracetic acid at −40 °C generates a highly reactive intermediate, 2b(PAA), that has the fastest rate to date for oxidizing cyclohexane by a nonheme iron species. It exhibits an intense 490 nm chromophore associated with an S = 1/2 EPR signal having g-values at 2.07, 2.01, and 1.94. This species was shown to be in a fast equilibrium with a second S = 1/2 species, 2a(PAA), assigned to a low-spin acylperoxoiron(III) center. Unfortunately, contaminants accompanying the 2(PAA) samples prevented determination of the iron oxidation state by Mossbauer spectroscopy. Use of MeO-PyNMe3 (an electron-enriched version of PyNMe3) and cyclohexyl pero…

Cyclohexane010405 organic chemistryReactive intermediateGeneral ChemistryChromophore010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceslaw.inventionchemistry.chemical_compoundColloid and Surface ChemistrychemistrylawOxidation stateMössbauer spectroscopyOxidizing agentPhysical chemistryElectron paramagnetic resonanceGround stateJournal of the American Chemical Society
researchProduct

Translational dynamics effects on the non-local correlations between two atoms

2005

A pair of atoms interacting successively with the field of the same cavity and exchanging a single photon, leave the cavity in an entangled state of Einstein-Podolsky-Rosen (EPR) type (see, for example, [S.J.D. Phoenix, and S.M. Barnett, J. Mod. Opt. \textbf{40} (1993) 979]). By implementing the model with the translational degrees of freedom, we show in this letter that the entanglement with the translational atomic variables can lead, under appropriate conditions, towards the separability of the internal variables of the two atoms. This implies that the translational dynamics can lead, in some cases, to difficulties in observing the Bell's inequality violation for massive particles.

DECOHERENCEVIOLATIONPhotonField (physics)SEPARABILITYCOMPLEMENTARITYDegrees of freedom (physics and chemistry)General Physics and AstronomyFOS: Physical sciencesQuantum entanglementType (model theory)QUANTUM STATElaw.inventionlawQuantum mechanicsElectron paramagnetic resonanceENTANGLEMENTPhysicsQuantum PhysicsDynamics (mechanics)BELL INEQUALITYState (functional analysis)Quantum PhysicsDEFLECTIONQuantum Physics (quant-ph)INTERFEROMETERTRANSITION
researchProduct