Search results for "spin [structure function]"

showing 10 items of 1132 documents

Competition of Direct and Indirect Sources of Thermal Entanglement in a spin star network

2017

A spin star system consisting of three peripheral two-state systems and a central one is considered, with the peripheral spins assumed to interact with each other, as well as with the central one. It is shown that such two couplings, each one being a thermal entanglement source, can significantly compete in the formation of quantum correlations in the thermal state, to the point that they can destroy any thermal entanglement of the peripheral spins.

Thermal entanglementPhysicsStar networkQuantum PhysicsPhysics and Astronomy (miscellaneous)Spinsspin networkFOS: Physical sciencesThermal entanglement01 natural sciencesspin systemSettore FIS/03 - Fisica Della Materia010305 fluids & plasmasQuantum mechanics0103 physical sciencesThermal stateSpin network010306 general physicsQuantum Physics (quant-ph)Nuclear ExperimentQuantumSpin-½
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Downsizing of robust Fe-triazole@SiO2 spin-crossover nanoparticles with ultrathin shells

2019

A chemical protocol to design robust hybrid [Fe(Htrz)2(trz)](BF4)@SiO2 nanoparticles (NPs) with sizes as small as 28 nm and ultrathin silica shells below 3 nm has been developed. These NPs present a characteristic abrupt spin transition with a subsequent decrease in the width of the thermal hysteresis upon reducing the NP size.

Thermal hysteresisMaterials science010405 organic chemistrySpin transitionTriazoleNanoparticleQuímica010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryChemical physicsSpin crossoverCompostos de coordinació
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Spin-crossover nanocrystals with magnetic, optical, and structural bistability near room temperature.

2008

ThermochromismNanostructureThermal hysteresisCondensed matter physicsNanocrystalBistabilitySpin crossoverMicroemulsionGeneral ChemistryGeneral MedicineMolecular materialsPhotochemistryCatalysisAngewandte Chemie (International ed. in English)
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The Two‐Step Spin Conversion in a Supramolecular Triple Helicate Dinuclear Iron(II) Complex Studied by Mössbauer Spectroscopy

2006

The triple helicate dinuclear iron(II) complex, [Fe-2(L)(3)](ClO4)(4)center dot 2H(2)O (1), previously reported by Tuna et al. (Chem. Eur. J. 2004, 10, 5737), was prepared and characterised by detailed SQUID and Fe-57 Mbssbauer measurements. Compound 1 exhibits a thermochromic two-step spin conversion at T-SC((1)) ca. 240 K and T-SC((2)) ca. 120 K, but does not switch its spin state further below 20 K as proven by Mossbauer spectroscopy. The sharp variation of the susceptibility below 20 K is due to zero-field splitting of the remaining iron(II) high-spin species. Applied field Fe-57 Mossbauer spectroscopy experiments at 4.2 K indicate that the gradual thermal spin conversion from [HS-HS] p…

ThermochromismSpin statesChemistryStereochemistryTwo stepSupramolecular chemistrylaw.inventionInorganic ChemistrySQUIDCrystallographySpin crossoverlawMössbauer spectroscopySpin (physics)European Journal of Inorganic Chemistry
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Thermal and Light-Induced Spin Transition in [Fe(bpen)X2] (bpen = 1,6-Bis(2-pyridyl)-2,5-diazahexane, X = NCS-, NCSe-)

1996

The thermal and light-induced spin transitions in [Fe(bpen)(NCS)2] and [Fe(bpen)(NCSe)2] have been investigated by means of magnetic susceptibility and Mossbauer measurements. The HS → LS transition in [Fe(bpen)(NCS)2] is detected at temperatures below 120 K (T1/2 [when the fraction of high-spin species γHS = 0.5] = 68 K) with a residual HS fraction of 8% at 20 K. The transition is fairly abrupt and no hysteresis is observed, in contrast to earlier studies (ref. [8]). The generation of metastable HS states in [Fe(bpen)(NCS)2] is achieved by rapid cooling of the sample and by irradiating the compound at low temperatures with light of appropriate wavelengths (LIESST). The HS → LS relaxation o…

ThiocyanateSpin statesOrganic ChemistryRelaxation (NMR)Spin transitionGeneral ChemistryMagnetic susceptibilityCatalysisLIESSTchemistry.chemical_compoundNuclear magnetic resonancechemistrySpin crossoverMössbauer spectroscopyPhysical chemistryChemistry - A European Journal
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Photomagnetism of a Series of Dinuclear Iron(II) Complexes

2009

International audience; The photomagnetic properties of a series of [{Fe(NCS)(py-X)}2(bpypz)2] (NCS=thiocyanate, py=pyridine, X=4-Mepy, py, 3-Mepy, 3-Clpy and 3-Brpy, and bpypz=3,5-bis(pyridine-2-yl)pyazolate) binuclear complexes are close to the antiferromagnetic response of [{Fe(NCS)(3,5-dmpy)}3(bpypz)2] (3,5-dmpy=3,5-dimethylpyrazine), which is characterised by two iron(II) metal ions in a high-spin (HS) electronic configuration . This paper describes the photomagnetic properties of a series of binuclear iron(II) complexes belonging to the [{Fe(NCS)(py-X)}2(bpypz)2] family (NCS=thiocyanate; py=pyridine; bpypz=3,5-bis(pyridine-2-yl)pyrazolate; and py-X=4-Mepy (1), py (3), 3-Mepy (4), 3-Cl…

ThiocyanateStereochemistryOrganic ChemistryHydrostatic pressureSpin transitionIron(II)[CHIM.MATE]Chemical Sciences/Material chemistry02 engineering and technologyGeneral ChemistrySpin crossover010402 general chemistry021001 nanoscience & nanotechnologyPhotomagnetism01 natural sciencesCatalysisLIESST0104 chemical scienceschemistry.chemical_compoundCrystallographychemistrySpin crossoverPyridineAntiferromagnetism0210 nano-technologyPhotomagnetismChemistry - A European Journal
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Abdominal and Thoracic Magnetic Resonance Angiography: Challenges, Technical Approaches, and First Clinical Applications

1993

The main goal of magnetic resonance angiography (MRA) is to enrich the huge potential of magnetic resonance imaging (MRI) by additional morphological and functional information about the vasculature. In spin echo sequences fast flowing blood leads to signal extinction, providing high contrast between tissue and vascular structures without the need for contrast media. However, various artifacts are frequently observed which alter the assessment of the vasculature. They are due to alterations of flow (slow velocity or turbulences) or induced by the acquisition technique (Mills et al. 1983; Bradley and Waluch 1985). By using gradient echo sequences, high-quality angiograms can be obtained from…

Thoraxmedicine.diagnostic_testComputer sciencemedia_common.quotation_subjectMagnetic resonance imagingInferior vena cavaMagnetic resonance angiographymedicine.anatomical_structuremedicine.veinmedicineSpin echoContrast (vision)AbdomenGradient echoBiomedical engineeringmedia_common
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Through-space spin-spin coupling in acetylenic systems. Ab initio and DFT calculations

2003

Abstract: We have investigated, by means of ab initio and DFT calculations, the magnitude of through-space spin-spin couplings ( J CH and J HH ) in CH/π bonded van der Waals dimers involving acetylene, and in a structurally related covalent compound (4-ethynylphenanthrene). Within regions where the interaction is stabilizing J HH couplings are very small (< 0.1 Hz) for all complexes. In the acetylene-methane complex J CH is also very small, whereas in the acetylene-benzene complex and the acetylene dimer it shows a relatively large dependence on the tilt angle from the T-shaped arrangement, for which the smallest values are calculated, to a parallel slipped arrangement where J CH is ca. 0.5…

Through-space couplingDimerAb initioDFTCatalysisspin-spin couplinglcsh:ChemistryInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeNMR spectroscopyComputational chemistryThrough-space coupling / NMR / ab initio / DFTPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryNMR spectroscopy; computational chemistry; spin-spin couplingSpin (physics)lcsh:QH301-705.5Molecular BiologySpectroscopyCouplingab initioChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopycomputational chemistryNMRComputer Science ApplicationsCrystallographylcsh:Biology (General)lcsh:QD1-999AcetyleneCovalent bondsymbolsCondensed Matter::Strongly Correlated ElectronsComputingMethodologies_GENERALvan der Waals force
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REDUCTION OF NILUTAMIDE BY NO SYNTHASES : IMPLICATIONS FOR THE ADVERSE EFFECTS OF THIS NITROAROMATIC ANTIANDROGEN DRUG

2003

Nitric oxide synthases (NOSs) are flavohemeproteins that catalyze the oxidation of l-arginine to l-citrulline with formation of the widespread signal molecule NO. Beside their fundamental role in NO biosynthesis, these enzymes are also involved in the formation of reactive oxygen species and in the interactions with some xenobiotic compounds. Nilutamide is a nonsteroidal antiandrogen that behaves as a competitive antagonist of the androgen receptors and is proposed in the treatment of metastatic prostatic carcinoma. However, therapeutic effects of nilutamide are overshadowed by the occurrence of several adverse reactions mediated by toxic mechanism(s), which remain(s) poorly investigated. H…

Time FactorsFree RadicalsNitric Oxide Synthase Type IIImedicine.drug_class[CHIM.THER] Chemical Sciences/Medicinal ChemistryNitric Oxide Synthase Type IINitric Oxide Synthase Type I[CHIM.THER]Chemical Sciences/Medicinal ChemistryToxicologyAntiandrogenImidazolidinesNitric oxide03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineHydroxylaminemedicineAnimalsAnaerobiosisAmines030304 developmental biologychemistry.chemical_classification0303 health sciencesReactive oxygen speciesElectron Spin Resonance SpectroscopyImidazolesAndrogen AntagonistsGeneral MedicineRecombinant Proteins3. Good healthRatsAndrogen receptorEnzymechemistryBiochemistryCompetitive antagonist030220 oncology & carcinogenesisNilutamideCattleNitric Oxide SynthaseOxidation-ReductionNADPmedicine.drug
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Real-Time Nuclear Magnetic Resonance Detection of Fumarase Activity Using Parahydrogen-Hyperpolarized [1- 13 C]Fumarate

2019

Hyperpolarized fumarate can be used as a probe of real-time metabolism in vivo, using carbon-13 magnetic resonance imaging. Dissolution dynamic nuclear polarization is commonly used to produce hyperpolarized fumarate, but a cheaper and faster alternative is to produce hyperpolarized fumarate via PHIP (parahydrogen-induced polarization). In this work, we trans-hydrogenate [1-13C]acetylene dicarboxylate with para-enriched hydrogen using a commercially available Ru catalyst in water to produce hyperpolarized [1-13C]fumarate. We show that fumarate is produced in 89% yield, with succinate as a side product in 11% yield. The proton polarization is converted into 13C magnetization using a constant…

Time FactorsHydrogenNuclear Magnetic Resonancechemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesBiochemistryCatalysisFumarate HydrataseCatalysisMagnetizationchemistry.chemical_compoundColloid and Surface ChemistryFumaratesMoleculeCarbon IsotopesMolecular StructureFumarase activityCarbon Isotopes; Fumarate Hydratase; Fumarates; Molecular Structure; Time Factors; Nuclear Magnetic Resonance BiomolecularGeneral Chemistry0104 chemical sciencesAcetylenechemistryFumaraseBiomolecularJournal of the American Chemical Society
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