Search results for "spin [structure function]"

showing 10 items of 1132 documents

Effect of tin and lead chlorotriphenyl analogues on fruit fly Drosophila hydei and liposomes membrane

2011

This article presents the results of a study investigating the biological activity of triphenyltin chloride (TPhT) and two metalloorganic compounds, triphenyllead chloride (TPhL) and triphenylmethane chloride (TPhC), in their interaction with model membranes and the living organisms of fruit flies Drosophila hydei. The study of model membranes (sonicated liposomes) was conducted using the electron spin resonance (ESR) spin probe technique, whereas the experiment on fruit flies involved investigating their viability on media containing the studied compounds. The test results clearly demonstrate that TPhT affects fruit flies more actively than TPhL (complete lethality after 7 days of culture …

Triphenyltin chlorideHealth Toxicology and MutagenesisToxicologyBiochemistryChloridechemistry.chemical_compoundOrganometallic CompoundsOrganotin CompoundsmedicineAnimalsLipid bilayerMolecular BiologyDrosophilaLiposomeTriphenylmethanebiologyCell MembranefungiElectron Spin Resonance SpectroscopyTrityl CompoundsGeneral Medicinebiology.organism_classificationMembraneLeadBiochemistrychemistryTinLiposomesModels AnimalDrosophila hydeiMolecular MedicineDrosophilamedicine.drugJournal of Biochemical and Molecular Toxicology
researchProduct

Effect of Chlorotriphenyl Derivatives of Sn and Pb upon Biophysical Properties of Membranes

2009

Biophysical activity of two twin organometallic compounds Triphenyltin chloride (TPhT) and Triphenyllead chloride (TPhL) in their interreaction with model membranes, as well as with yeast cellsSaccharomyces cerevisiae, was investigated. Four measurement methods were used in the experiments: two physical methods (spin probes method and the electric method); two biological methods (minimal inhibitory concentration /MIC/ and yeast survival test). It has been found that the activity of TPhT in interaction with model membranes and yeast cells is distinctly greater than that of TPhL. The activity manifests itself by considerable increase in the fluidity of the middle part of liposome bilayer, cha…

Triphenyltin chlorideTime FactorsArticle SubjectCell SurvivalHealth Toxicology and Mutagenesislcsh:BiotechnologySaccharomyces cerevisiaelcsh:MedicineSaccharomyces cerevisiaelcsh:Chemical technologylcsh:TechnologyBiophysical PhenomenaMembrane PotentialsCell membranechemistry.chemical_compoundlcsh:TP248.13-248.65GeneticsmedicineOrganometallic CompoundsOrganotin Compoundslcsh:TP1-1185Molecular BiologyLiposomebiologyChemistrylcsh:TBilayerCell Membranelcsh:RElectron Spin Resonance SpectroscopyLauric AcidsGeneral Medicinebiology.organism_classificationLauric acidYeastMembranemedicine.anatomical_structureBiochemistryLiposomesBiophysicsMolecular MedicineBiotechnologyResearch ArticleJournal of Biomedicine and Biotechnology
researchProduct

Unusual packing of ET molecules caused by π–π stacking interactions with TRISPHAT molecules in two [ET][TRISPHAT] salts (ET=bis(ethylenedithio)tetrat…

2007

Abstract The synthesis, structure and physical properties of two new radical salts formed with the organic donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF or ET) and a racemic mixture of the chiral anion (tris(tetrachlorobenzenediolato)phosphate(V)) (TRISPHAT) are reported. The structure of the salts (ET)4[TRISPHAT]4 · 3.5H2O (1) and (ET)(TRISPHAT) · CH2Cl2 · CH3CN (2) has been solved by X-ray single crystal diffraction. Unusual packings of ET molecules are obtained in the two structures. The electrical properties indicate that both compounds are insulators. This is in agreement with the isolation of the ET molecules and their complete ionization. On the other hand, the anisotropy of …

TrisConductivityCrystal structureInorganic chemistryTRISPHATStackingCrystal structureIonInorganic Chemistrychemistry.chemical_compoundCrystallographyTRISPHATchemistryddc:540Materials ChemistryRacemic mixtureMoleculeElectrocrystallisationTTF-based radical saltsElectronic spin resonancePhysical and Theoretical ChemistryTetrathiafulvaleneInorganica Chimica Acta
researchProduct

Nanosession: Spin Tunneling Systems

2013

Tunnel magnetoresistanceMaterials scienceCondensed matter physicsResistive switchingSpin tunnelingAntiferromagnetic coupling
researchProduct

Purification and spectroscopic studies on catechol oxidases from Lycopus europaeus and Populus nigra: evidence for a dinuclear copper center of type …

1999

We purified two catechol oxidases from Lycopus europaeus and Populus nigra which only catalyze the oxidation of catechols to quinones without hydroxylating tyrosine. The molecular mass of the Lycopus enzyme was determined to 39,800 Da and the mass of the Populus enzyme was determined to 56,050 Da. Both catechol oxidases are inhibited by thiourea, N-phenylthiourea, dithiocarbamate, and cyanide, but show different pH behavior using catechol as substrate. Atomic absorption spectrosopic analysis found 1.5 copper atoms per protein molecule. Using EPR spectroscopy we determined 1.8 Cu per molecule catechol oxidase. Furthermore, EPR spectroscopy demonstrated that catechol oxidase is a copper enzym…

TyrosinaseCatecholschemistry.chemical_elementPhotochemistrySpectrum Analysis RamanBiochemistrylaw.inventionTreesInorganic Chemistrychemistry.chemical_compoundlawPolymer chemistryEnzyme InhibitorsElectron paramagnetic resonanceCatechol oxidaseCatecholBinding SitesCyanidesbiologyMonophenol MonooxygenaseSpectrophotometry AtomicElectron Spin Resonance SpectroscopySubstrate (chemistry)Bridging ligandHydrogen-Ion ConcentrationPlantsPhenylthioureaCopperMolecular WeightchemistryHemocyaninsbiology.proteinSpectrophotometry UltravioletOxygen bindingCatechol OxidaseCopperJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
researchProduct

Angular momentum population in fragmentation reactions

2009

Neutron-deficient nuclei with N = 126 have been populated following projectile fragmentation of a 238U beam with energy 1 GeV/A. The decay of several previously reported isomers has been measured. This will allow us to calculate high-spin isomeric ratios and compare them with model calculations to allow a better understanding of the reaction mechanism. Algora, Alejandro, Alejandro.Algora@ific.uv.es ; Molina Palacios, Francisco Manuel, Francisco.Molina@ific.uv.es ; Rubio Barroso, Berta, Berta.Rubio@ific.uv.es

UNESCO::FÍSICA::Física molecular:FÍSICA [UNESCO]:FÍSICA::Física molecular [UNESCO]UNESCO::FÍSICANeutron-deficient nucleiProjectile fragmentationHigh-spin isometric ratiosNeutron-deficient nuclei ; Projectile fragmentation ; High-spin isometric ratios ; Reaction mechanismReaction mechanism
researchProduct

[Fe(sal2-trien)][Ni(dmit)2]: towards switchable spin crossover molecular conductors

2004

A cooperative spin transition behaviour with a wide hysteresis loop (30 K) around 240 K has been observed, for the first time, in a salt based on the redox active [Ni(dmit)2]¯, anion and the [Fe(sal2-trien)]+ spin crossover cation. Real Cabezos, Jose Antonio, Jose.A.Real@uv.es

UNESCO::QUÍMICASpin transitionSalt (chemistry)Mineralogy:QUÍMICA [UNESCO]Fe(sal2-trien)][Ni(dmit)2CatalysisIonSpin crossoverMaterials ChemistryRedox activeElectrical conductorchemistry.chemical_classificationMolecular conductorsUNESCO::QUÍMICA::Química inorgánicaMolecular conductors ; Spin transition ; Salt based ; Fe(sal2-trien)][Ni(dmit)2Metals and AlloysSpin transitionSalt basedGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositesChemical Communications
researchProduct

Magnetic mixed-valence d2-d1-d1 trimers with partial electron delocalization: vibronic coupling and magnetic properties

1993

Abstract The energy levels and magnetic properties of a triangular mixed-valence cluster d1-d1-d2 with electron delocalization in a pair of sites are examined from a model that takes into account electron transfer, magnetic exchange, and vibronic coupling. We show that the electron transfer process involves besides the usual double-exchange parameter, and additional parameter referred to as exchange transfer. This last parameter accounts for the interaction between the moving electron of the mixed valence pair and the electron localized in the third side. We notice that the role of double exchange is to stabilize a ferromagnetic alignment of the spins on the mixed-valence pair. A comparison…

Valence (chemistry)Condensed matter physicsSpin statesChemistryGeneral Physics and AstronomyElectronDelocalized electronElectron transferVibronic couplingFerromagnetismPhysics::Atomic and Molecular ClustersAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryChemical Physics
researchProduct

Electric field control of the optical properties in magnetic mixed-valence molecules

2014

We propose the use of an electric field stimulus to strongly affect the optical properties of ferromagnetic mixed-valence (MV) dimers. This proposal is based on the prediction of an anomalous Stark effect in the intervalence absorption bands of these multi-electron MV systems. As distinguished from the conventional Stark effect observed in one-electron dimers, a strong change of the intervalence bands accompanies the crossing of the different spin levels caused by the application of an electric field. This new effect can be referred to as giant spin-dependent Stark effect. In spintronics this opens up the possibility for optical detection of the spin state in these magnetic molecules.

Valence (chemistry)Condensed matter physicsSpintronicsSpin statesChemistryQuantum-confined Stark effectGeneral Chemistrysymbols.namesakeStark effectFerromagnetismElectric fieldPhysics::Atomic and Molecular ClusterssymbolsMoleculeCondensed Matter::Strongly Correlated ElectronsChem. Sci.
researchProduct

Mixed-valence polyoxometalate clusters. I. Delocalization of electronic pairs in dodecanuclear heteropoly blues with keggin structure

1995

Abstract The problem of delocalization of a pair of electrons over dodecanuclear polyoxometalate clusters with the Keggin structure is considered with the aim of explaining the spin pairing in these multi-nuclear mixed-valence systems. A general approach that considers the Coulomb interactions between the two delocalized electrons, as well as the single and double electron transfer processes which can be operative in delocalization of the electronic pairs is developed. The new approach is based on the site-symmetry concept which makes possible a group theoretical classification for the delocalized states of electronic pairs. This procedure proves to be very efficient in the calculation of t…

Valence (chemistry)Spin statesGeneral Physics and AstronomyMolecular physicsDelocalized electronKeggin structurechemistry.chemical_compoundchemistryPairingPolyoxometalateCluster (physics)Singlet statePhysical and Theoretical ChemistryAtomic physicsChemical Physics
researchProduct