Search results for "spin [structure function]"

showing 10 items of 1132 documents

Spin Transition in Iron Compounds

1984

First-row transition metal complexes with d4 up to d7 electron configuration in octahedral ligand fields (and d8 electron configuration in six-coordinate complexes of lower symmetry) may undergo temperature dependent high spin (HS) ⇌ low spin (LS) transition, provided the ligand field strength (Δ), including low symmetry contributions, becomes comparable in magnitude with the mean spin pairing energy (P). At a critical field strength Δcrit = P, the energy levels of the two spin states cross. This is illustrated in Fig. 1, where a simplified Tanabe-Sugano type energy level diagram for d6 systems (e.g. Fe2+, Co3+) is shown as an example. For weak ligand fields, Δ Δcrit, the LS state1A1g(Oh) b…

Physicssymbols.namesakeSpin statesTransition metalSpin crossoverSpin transitionsymbolsElectron configurationMolecular physicsCritical fieldSpin-½Gibbs free energy
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High-spin states in the neutron-rich A∼100 region

2009

Two experimental setups have been used to study excited states of neutron‐rich nuclei in the A∼100 region. Extended level schemes and lifetime measurements were obtained using deep‐inelastic and fusion‐fission reactions with the CLARA‐PRISMA spectrometer and the Ge‐array GASP respectively. Experimental information from GASP has been used to complement the CLARA‐PRISMA experiment. Time spectra have been used to measure the lifetimes of isomeric states. Preliminary results are presented for 89Rb.

Physicsγ-ray transitionsSpin statesSpectrometerAstrophysics::High Energy Astrophysical PhenomenaLifetimesPRISMA-CLARA spectrometerGASP arrayDeep inelastic scatteringSpectral lineNuclear physicsPhysics and Astronomy (all)Excited stateNuclear fusionNeutronGamma spectroscopyAtomic physicsγ-ray transitions; GASP array; Lifetimes; PRISMA-CLARA spectrometer; Physics and Astronomy (all)Nuclear ExperimentAIP Conference Proceedings
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A Heterobimetallic Anionic 3,6-Connected 2D Coordination Polymer Based on Nitranilate as Ligand

2016

In order to synthesize new coordination polymers with original architectures and interesting magnetic properties, we used the nitranilate ligand (C₆O₄(NO₂)₂2- = C₆N₂O₈2-), derived from the dianionic ligand dhbq2- (2,5-dihydroxy-1,4-benzoquinone = H₂C₆O₄2-). The use of this bis-bidentate bridging ligand led to [(DAMS)₂{FeNa(C₆N₂O₈)₃}·CH₃CN]n (1) (DAMS⁺ = C16H17N₂⁺ = 4-[4-(dimethylamino)-α-styryl]-1-methylpyridinium), a 2D heterometallic coordination polymer presenting an unprecedented structure for any anilato-based compound. This structural type is a 3,6-connected 2D coordination polymer derived from the well-known honeycomb hexagonal structure, where Fe(III) ions alternate with Na⁺ dimers …

Polymers and PlasticsCoordination polymerStereochemistryZero field splitting010402 general chemistry01 natural sciencesArticleIonlcsh:QD241-441Paramagnetismchemistry.chemical_compoundlcsh:Organic chemistrymagnetic properties high spin Fe(III) complexchemistry.chemical_classificationanilato ligands; heterometallic; coordination polymers; magnetic properties high spin Fe(III) complex010405 organic chemistryLigandCenter (category theory)Bridging ligandGeneral ChemistryPolymer0104 chemical sciencesCrystallographycoordination polymerschemistryheterometallicanilato ligandsPolymers; Volume 8; Issue 3; Pages: 89
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Aggregation behavior of amphiphilic p(HPMA)-co-p(LMA) copolymers studied by FCS and EPR spectroscopy.

2012

A combined study of fluorescence correlation spectroscopy and electron paramagnetic resonance spectroscopy gave a unique picture of p(HPMA)-co-p(LMA) copolymers in aqueous solutions, ranging from the size of micelles and aggregates to the composition of the interior of these self-assembled systems. P(HPMA)-co-p(LMA) copolymers have shown high potential as brain drug delivery systems, and a detailed study of their physicochemical properties can help to elucidate their mechanism of action. Applying two complementary techniques, we found that the self-assembly behavior as well as the strength of hydrophobic attraction of the amphiphilic copolymers can be tuned by the hydrophobic LMA content or…

Polymers and PlasticsPolymersBioengineeringFluorescence correlation spectroscopyMicelleModels Biologicallaw.inventionBiomaterialsSurface-Active AgentsDrug Delivery SystemslawPolymer chemistryAmphiphileMaterials ChemistrySide chainCopolymerElectron paramagnetic resonanceAlkylMicelleschemistry.chemical_classificationChemistryElectron Spin Resonance SpectroscopyDomperidoneHydrophobeSpectrometry FluorescenceLiposomesMethacrylatesHydrophobic and Hydrophilic InteractionsBiomacromolecules
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Oxidative Addition of Halogens on Open Metal Sites in a Microporous Spin-Crossover Coordination Polymer

2009

PolymersCoordination polymeroxidative additionMolecular ConformationchemisorptionPhotochemistryCatalysisMetalchemistry.chemical_compoundHalogensX-Ray Diffractionspin crossoverSpin crossoverPlatinumporous compoundsBinding SitesGeneral ChemistryMicroporous materialGeneral MedicineOxidative additioncoordination polymerschemistryMetalsChemisorptionvisual_artX-ray crystallographyHalogenvisual_art.visual_art_mediumOxidation-ReductionAngewandte Chemie
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Coordination polymers undergoing spin crossover and reversible ligand exchange in the solid

2006

Here we report the synthesis and characterisation of a polymer made up of a system of parallel 2-D grids of Fe(II) ions linked by [Au(CN)2]– bridges and its transformation into a new system of three interpenetrated 3-D coordination open frameworks with the NbO topology. Reversibility of this crystal-to-crystal transformation is evidenced by X-ray crystallographic data and from their spin crossover properties. Real Cabezos, Jose Antonio, Jose.A.Real@uv.es

PolymersUNESCO::QUÍMICACrystallographic data:QUÍMICA [UNESCO]CatalysisIonSynthesisSpin crossoverMaterials ChemistryTopology (chemistry)chemistry.chemical_classificationLigandUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryPolymerX-Ray crystallographicSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoordination ; Polymers ; Synthesis ; NbO topology ; X-Ray crystallographicCrystallographychemistryCoordination:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesNbO topologyNatural bond orbital
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Spin crossover properties of the [Fe(PM-BiA)2(NCS)2] complex - phases I and II

2003

International audience; In the present review, we reexamine the photomagnetic properties of the [Fe(PM-BiA)2(NCS)2], cis-bis(thiocyanato)-bis[(N-2'-pyridylmethylene)-4-(aminobiphenyl)]iron(II), compound which exhibits, depending on the synthetic method, an exceptionally abrupt spin transition (phase I) with a very narrow hysteresis (T1/2O = 168 K and T1/2N = 173 K) or a gradual spin conversion (phase II) occurring at 190 K. In both cases, light irradiation in the tail of the 1MLCT-LS absorption band, at 830 nm, results in the population of the high-spin state according to the light-induced excited spin-state trapping (LIESST) effect. The capacity of a compound to retain the light-induced HS…

PopulationAnalytical chemistrySpin transition02 engineering and technology010402 general chemistry01 natural sciencesLIESSTSpin crossoverPhase (matter)educationKinetic relaxationeducation.field_of_studyCondensed matter physicsChemistryGeneral ChemistryIron(II)[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPhotomagnetismSpin crossover0104 chemical sciencesKinetic relaxation.HysteresisExcited state0210 nano-technologyPhotomagnetism
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Zn-Enhanced Asp-Rich Antimicrobial Peptides N-Terminal Coordination by Zn(II) and Cu(II), Which Distinguishes Cu(II) Binding to Different Peptides

2021

The antimicrobial activity of surfactant-associated anionic peptides (SAAPs), which are isolated from the ovine pulmonary surfactant and are selective against the ovine pathogen Mannheimia haemolytica, is strongly enhanced in the presence of Zn(II) ions. Both calorimetry and ITC measurements show that the unique Asp-only peptide SAAP3 (DDDDDDD) and its analogs SAAP2 (GDDDDDD) and SAAP6 (GADDDDD) have a similar micromolar affinity for Zn(II), which binds to the N-terminal amine and Asp carboxylates in a net entropically-driven process. All three peptides also bind Cu(II) with a net entropically-driven process but with higher affinity than they bind Zn(II) and coordination that involves the N…

Pore Forming Cytotoxic Proteins0301 basic medicineStereochemistryQH301-705.5Metal ions in aqueous solutionAntimicrobial peptidesPeptide010402 general chemistry01 natural sciencesArticleCatalysisInorganic Chemistry03 medical and health scienceschemistry.chemical_compoundthermodynamicsDeprotonationZn(II) and Cu(II) bioinorganic chemistryPulmonary surfactantAmidePhysical and Theoretical ChemistryBiology (General)Mannheimia haemolyticaMolecular BiologyQD1-999Spectroscopychemistry.chemical_classificationOrganic ChemistryElectron Spin Resonance SpectroscopyGeneral Medicine0104 chemical sciencesComputer Science ApplicationsZincChemistry030104 developmental biologyMembranechemistryAmine gas treatingmetal-antimicrobial peptide interactionsPeptidesCopperInternational Journal of Molecular Sciences
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Novel Iron(II) Microporous Spin-Crossover Coordination Polymers with Enhanced Pore Size

2012

In this Communication, we report the synthesis and characterization of novel Hofmann-like spin-crossover porous coordination polymers of composition {Fe(L)[M(CN)4]}·G [L = 1,4-bis(4-pyridylethynyl)- benzene and MII = Ni, Pd, and Pt]. The spin-crossover properties of the framework are closely related to the number and nature of the guest molecules included in the pores.

Pore sizeModels MolecularPolymersSurface PropertiesInorganic chemistryConductivityInorganic ChemistryCrystalchemistry.chemical_compoundSpin crossoverMemory devicesCrystalMoleculeFerrous CompoundsPhysical and Theoretical ChemistryParticle SizeBenzenechemistry.chemical_classificationConductivityTemperatureMicroporous materialPolymerCrystallographychemistryFISICA APLICADATransitionPorosityFramework material
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Porphyrin amino acids-amide coupling, redox and photophysical properties of bis(porphyrin) amides.

2013

New trans-AB2C meso-substituted porphyrin amino acid esters with meso-substituents of tunable electron withdrawing power (B = mesityl, 4-C6H4F, 4-C6H4CF3, C6F5) were prepared as free amines 3a-3d, as N-acetylated derivatives Ac-3a-Ac-3d and corresponding zinc(II) complexes Zn-Ac-3a-Zn-Ac-3d. Several amide-linked bis(porphyrins) with a tunable electron density at each porphyrin site were obtained from the amino porphyrin precursors by condensation reactions (4a-4d) and mono- and bis(zinc(II)) complexes Zn(2)-4d and Zn(1)Zn(2)-4d were prepared. The electronic interaction between individual porphyrin units in bis(porphyrins) 4 is probed by electrochemical experiments (CV, EPR), electronic abso…

PorphyrinsAbsorption spectroscopyMetalationchemistry.chemical_elementZincPhotochemistryRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawAmidePolymer chemistryOrganometallic CompoundsAmino AcidsElectron paramagnetic resonanceMolecular StructureElectron Spin Resonance SpectroscopyCondensation reactionPhotochemical ProcessesPorphyrinAmidesZincchemistryQuantum TheoryOxidation-ReductionDalton transactions (Cambridge, England : 2003)
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