Search results for "Films"

showing 10 items of 2839 documents

[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
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Coexistence of ferro- and antiferromagnetic interactions in a metal-organic radical-based (6,3)-helical network with large channels.

2005

A metal–organic open-framework with an unprecedented (6,3)-helical topology, large channels and mixed ferro- and antiferromagnetic interactions has been synthesized using a three-connecting tricarboxylic polychlorotriphenylmethyl radical and Co(II) ions. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

UNESCO::QUÍMICA::Química inorgánicaChemistryUNESCO::QUÍMICAMetals and AlloysMetal-organicMineralogyGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSintetitzationFerro and antiferromagnetic ; Metal-organic ; Coexistence ; Tricarboxylic polychlorotriphenylmethyl radical ; SintetitzationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonChemical physicsMaterials ChemistryCeramics and CompositesAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsTricarboxylic polychlorotriphenylmethyl radicalFerro and antiferromagneticTopology (chemistry)CoexistenceChemical communications (Cambridge, England)
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UV photoexcitation of a dissolved metalloid Ge9 cluster compound and its extensive ultrafast response.

2015

Femtosecond pump-probe absorption spectroscopy in tetrahydrofuran solution has been used to investigate the dynamics of a metalloid cluster compound {Ge9[Si(SiMe3)3]3}(-). Upon UV photoexcitation, the transients in the near-infrared spectral region showed signatures reminiscent of excess electrons in THF (bound or quasi-free) whereas in the visible part excited state dynamics of the cluster complex dominates.

UV photoexcitationgermanium clustersAbsorption spectroscopyMetals and AlloysGeneral ChemistryElectronPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPhotoexcitationchemistry.chemical_compoundchemistryExcited stateFemtosecondMaterials ChemistryCeramics and CompositesCluster (physics)Metalloidta116TetrahydrofuranChemical communications (Cambridge, England)
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On the Deactivation Mechanisms of Adenine–Thymine Base Pair

2012

In this contribution, the multiconfigurational second-order perturbation theory method based on a complete active space reference wave function (CASSCF/CASPT2) is applied to study all possible single and double proton/hydrogen transfers between the nucleobases in the adenine-thymine (AT) base pair, analyzing the role of excited states with different nature [localized (LE) and charge transfer (CT)], and considering concerted as well as step-wise mechanisms. According to the findings, once the lowest excited states, localized in adenine, are populated during UV irradiation of the Watson-Crick base pair, the proton transfer in the N-O bridge does not require high energy in order to populate a …

Ultraviolet RaysBase pair02 engineering and technology010402 general chemistry01 natural sciencesReference wavechemistry.chemical_compoundQuantum mechanicsMaterials ChemistryComplete active spacePhysical and Theoretical ChemistryPerturbation theoryBase PairingAdenineFunction (mathematics)021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsThymineBIOFLAVONOIDESchemistryProtonsAtomic physics0210 nano-technologyThymineHydrogenThe Journal of Physical Chemistry B
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Unprecedented use of silver(I) N-heterocyclic carbene complexes for the catalytic preparation of 1,2-bis(boronate) esters.

2005

Catalytic diboration of internal and terminal alkenes with Ag(I) N-heterocyclic carbene complexes leads to 1,2-bis(boronate) esters as single intermediates, that can be oxidised towards the corresponding diols. Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es

UnprecedentedCatalytic diboration ; N-heterocyclic carbene ; Unprecedented ; SilverSilverUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysCatalytic diborationGeneral ChemistryGeneral Medicine:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCeramics and CompositesOrganic chemistryUNESCO::QUÍMICA::Química orgánicaN-heterocyclic carbeneCarbeneChemical communications (Cambridge, England)
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Chemical effect on the XPS spectra of the valence band and on O KLL and Pd MNN Auger spectra in pumice-supported catalysts

1992

X-ray photoelectron spectra of the valence band and X-ray-excited O KLL Auger transition of pumice-supported Pd and Pt catalysts have been obtained and compared to the corresponding spectra of pumice (a naturally occurring amorphous aluminosilicate). The changes observed indicate interaction between metal and support. The valence region of the catalysts consists of three large peaks: one due to the d band of the metals and the other to the O 2p non-bonding orbitals and bonding-type orbitals formed by a mixing of the atomic orbitals (O 2p, Si 3s and Si 3p) of oxygen and silicon from the support. The intensity decrease of the component due to the bonding orbitals, observed in the catalyst spe…

Valence (chemistry)ChemistryAnalytical chemistrySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsAugerAmorphous solidCondensed Matter::Materials ScienceX-ray photoelectron spectroscopyTransition metalAtomic orbitalAluminosilicatePhysics::Atomic and Molecular ClustersMaterials ChemistryMolecular orbitalSurface and Interface Analysis
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Spin Switching in Molecular Quantum Cellular Automata Based on Mixed-Valence Tetrameric Units

2016

In this article we focus on the study of spin effects in a single square-planar mixed-valence cell comprising two electrons and in coupled molecular cells for quantum cellular automata. Using the vibronic model we demonstrate that the polarizabilities of the cell are different in spin-singlet and spin-triplet states of the electronic pair. Based on this inference the concept of spin switching in molecular quantum cellular automata is proposed, and the conditions under which this effect is feasible are derived. In order to reveal these conditions we have performed a series of quantum-mechanical calculations of the vibronic energy levels of the isolated cell and of the cell subjected to the e…

Valence (chemistry)ChemistryQuantum dot cellular automaton02 engineering and technologyElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergySwitching cycleQuantum mechanicsPotential curvesPhysical and Theoretical Chemistry0210 nano-technologyAdiabatic processQuantum cellular automatonIsolated cellThe Journal of Physical Chemistry C
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Photomagnetic effect in a cyanide-bridged mixed-valence {FeII2FeIII2} molecular square

2012

The self-assembly of [Fe(III)(Tp)(CN)(3)](-) and [Fe(II)(bik)(2)(S)(2)](2+) affords the cyanide-bridged mixed valence {Fe(III)(2)Fe(II)(2)}(2+) molecular square, which exhibits a photomagnetic effect under laser light irradiation at low temperature and also shows thermal spin-state conversion near ambient temperature.

Valence (chemistry)Condensed matter physicsCyanideMetals and AlloysAnalytical chemistryPhotomagnetic effectGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryThermalMaterials ChemistryCeramics and CompositesIrradiationLaser lightChemical Communications
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Spin-resolved low-energy and hard x-ray photoelectron spectroscopy of off-stoichiometric Co2MnSi Heusler thin films exhibiting a record TMR

2015

Half-metallic Co2MnSi-based Heusler compounds have attracted attention because they yield very high tunnelling magnetoresistance (TMR) ratios. Record TMR ratios of 1995% (at 4.2 K) are obtained from off-stoichiometric Co2MnSi-based magnetic tunnel junctions. This work reports on a combination of band structure calculations and spin-resolved and photon-polarisation-dependent photoelectron spectroscopy for off-stoichiometric Heusler thin films with the composition Co2Mn1.30Si0.84. Co and Mn are probed by magnetic dichroism in angle-resolved photoelectron spectroscopy at the 2p core level. In contrast to the delocalised Co 3d states, a pronounced localisation of the Mn 3d states is deduced fro…

Valence (chemistry)Materials scienceAcoustics and UltrasonicsCondensed matter physicsMagnetoresistanceFermi energyDichroismPhoton energyCondensed Matter PhysicsLinear dichroismSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceX-ray photoelectron spectroscopyCondensed Matter::Strongly Correlated ElectronsElectronic band structureJournal of Physics D: Applied Physics
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Physical properties of (1−x)Ba0.95Pb0.05TiO3+xCo2O3 (x=0, 0.1, 0.3, 0.5, 1.0, 2.0wt%) ceramics

2015

The paper reports studies of the (1−x)Ba0.95Pb0.05TiO3 – xCo2O3 (x≤0.02) ceramics. Results of X-ray powder diffraction, dielectric, magnetic and IR measurements, as well as ab initio simulations are presented. The Co-doping induces small decrease of the (c/a) tetragonality of the perovskite lattice and leads to the gradual shift of the ferroelectric transition temperature from 398 K for x=0 down to 357 K for x=0.02. The conductivity activation energies are in the range 0.8–0.9 eV in agreement with the calculations. The high-temperature conductivity can be ascribed by the migration of oxygen vacancies introduced to compensate the charge deficiency due to Co3+ valence at the B-site of the per…

Valence (chemistry)Materials scienceCondensed matter physicsProcess Chemistry and TechnologyTransition temperatureAb initioDielectricConductivityFerroelectricitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMaterials ChemistryCeramics and CompositesMultiferroicsPowder diffractionCeramics International
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