Search results for "molecular electronic"

showing 10 items of 126 documents

The Dalton quantum chemistry program system

2013

Dalton is a powerful general-purpose program system for the study of molecular electronic structure at the Hartree-Fock, Kohn-Sham, multiconfigurational self-consistent-field, MOller-Plesset, confi ...

Physics::Computational PhysicsPhysicsNuclear TheoryBiochemistryQuantum chemistryComputer Science ApplicationsComputational MathematicsComputational chemistryAb initio quantum chemistry methodsQuantum mechanicsMolecular electronic structurePhysics::Atomic and Molecular ClustersMaterials ChemistryPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryWiley Interdisciplinary Reviews: Computational Molecular Science
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Alternating, all-trans polyenynes: Model compounds for poly(diacetylene)s with defined conjugation length

1994

The syntheses of polyenynes as model compounds for poly(diacetylene)s (PDAs) are described. Variation of properties (UV–VIS, Raman, NMR and bond geometries) as a function of the chain length was investigated. After extrapolation to infinite chain length these data were compared to those for PDAs. From UV–VIS spectra a value of λ = 551 nm (2.25 eV) was calculated corresponding to the electronic transition of a single polyenyne chain. This energy is located at the low energy end of a yellow PDA solution spectrum. From Raman scattering v(CC) = 2108–2128 cm−1 and v(CC) = 1505–1532 cm−1 were calculated after extrapolation. Similarly sp-C13C NMR data yielded a shift of δ = 100 ppm. These data are…

Polymers and PlasticsDiacetyleneChemistryStereochemistryOrganic ChemistryExtrapolationSpectral lineMolecular electronic transitionBond lengthchemistry.chemical_compoundsymbols.namesakeCrystallographyChain (algebraic topology)Materials ChemistrysymbolsRaman spectroscopyRaman scatteringPolymer International
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Computation of conical intersections by using perturbation techniques

2005

Multiconfigurational second-order perturbation theory, both in its single-state multiconfigurational second-order perturbation theory (CASPT2) and multistate (MS-CASPT2) formulations, is used to search for minima on the crossing seams between different potential energy hypersurfaces of electronic states in several molecular systems. The performance of the procedures is tested and discussed, focusing on the problem of the nonorthogonality of the single-state perturbative solutions. In different cases the obtained structures and energy differences are compared with available complete active space self-consistent field and multireference configuration interaction solutions. Calculations on dif…

Potential Energy SurfacesConfiguration Interactions ; Perturbation Theory ; Potential Energy Surfaces ; Molecular Electronic States ; SCF Calculations ; Lithium Compounds ; Organic Compounds ; Wave FunctionsOrganic CompoundsChemistryComputationUNESCO::FÍSICAConfiguration InteractionsGeneral Physics and AstronomyMultireference configuration interactionConical surfaceSCF CalculationsPotential energyWave FunctionsMaxima and minima:FÍSICA [UNESCO]Molecular Electronic StatesQuantum mechanicsPerturbation TheoryLithium CompoundsStatistical physicsComplete active spacePerturbation theory (quantum mechanics)Physical and Theoretical ChemistryWave functionThe Journal of Chemical Physics
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A theoretical study of the gas-phase chemi-ionization reaction between uranium and oxygen atoms

2005

The U+O chemi-ionization reaction has been investigated by quantum chemical methods. Potential-energy curves have been calculated for several electronic states of UO and UO+. Comparison with the available spectroscopic and thermodynamic values for these species is reported and a mechanism for the chemi-ionization reaction U+O -> UO++e(-) is proposed. The U+O and Sm+O chemi-ionization reactions are the first two metal-plus-oxidant chemi-ionization reactions to be studied theoretically in this way.

Quantum chemicalMolecular electronic statesChemistryGeneral Physics and Astronomychemistry.chemical_elementUraniumOxygenElectronic statesGas phaseOxygenAtom-atom reactionsAssociative ionisationOxygen atomPotential energy surfacesIonizationddc:540Reaction kinetics theoryPhysics::Atomic and Molecular ClustersUraniumPhysical chemistryPhysics::Atomic PhysicsPhysical and Theoretical ChemistryNuclear ExperimentChain reactionUranium compoundsThe Journal of Chemical Physics
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Improved stability of solid state light emitting electrochemical cells consisting of ruthenium and iridium complexes

2006

ABSTRACTTwo charged organometallic complexes containing bulky hydrophobic ligands based on ruthenium (II) and iridium (III) were synthesized and their performance in solid state light emitting electrochemical cells is described. The complexes were chosen as due to their large ligands a diminished susceptibility towards the formation of destructive complexes during device operation is expected. The LEC device performances reveal the longest living devices reported so far under dc bias. Quantum chemical calculations confirm that the major effect of the bulky diphenylphenanthroline ligands is of steric origin and not related with changes in the molecular electronic structure of the complexes.

Quantum chemicalSteric effectsMaterials sciencechemistryMolecular electronic structureSolid-statechemistry.chemical_elementIridiumPhotochemistryElectrochemical cellRuthenium
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Transition probabilities of PrII-lines emitted from a ferroelectric plasma source

1991

Abstract An argon-praseodymium plasma was generated under atmospheric pressure between a ceramic ferroelectric plate and a praseodymium plate. The system of plates was connected to an acoustic frequency supply. The plasma radiation was analyzed in the spectral range from 2000 to 7000 A by using a grating spectrograph with a linear dispersion near 1 mm/A, adopted to photoelectric measurements. The emission spectrum of praseodymium was recorded and the intensities of a few hundred lines were measured. Transition probabilities were determined for 62PrII-lines, using available lifetime data for excited levels and measured branching ratios of the corresponding lines. Reasonable agreement has bee…

RadiationMaterials sciencePraseodymiumchemistry.chemical_elementPlasmaPhotoelectric effectFerroelectricityAtomic and Molecular Physics and OpticsMolecular electronic transitionSpectral linechemistryExcited stateEmission spectrumAtomic physicsSpectroscopyJournal of Quantitative Spectroscopy and Radiative Transfer
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Facile approaches to build ordered amphiphilic tris(phthalocyaninato) europium triple-decker complex thin films and their comparative performances in…

2010

Solution processed thin films of an amphiphilic tris(phthalocyaninato) rare earth triple-decker complex, Eu(2)[Pc(15C5)(4)](2)[Pc(OC(10)H(21))(8)], have been prepared from three different methods: self-assembly (SA) annealed in solvent vapor, quasi-Langmuir-Shäfer (QLS) and drop casting methods. In particular, we successfully developed a simple QLS process for fabricating ordered multilayers with a good thickness control. The films prepared from three different methods were characterized by a wide range of methods including electronic absorption spectra, IR, X-ray diffraction, atomic force microscopy (AFM), and current-voltage (I-V) measurements. J-type aggregates have been formed with the …

Reaction rate constantchemistryAbsorption spectroscopyX-ray crystallographyStackingAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementSelf-assemblyPhysical and Theoretical ChemistryThin filmEuropiumMolecular electronic transitionPhysical Chemistry Chemical Physics
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Transition Dipole Orientation of Linear Polyenes:  Semiempirical Models and Extrapolation to the Infinite Chain Limit

1999

Linear conjugated polyenes have an electronic transition dipole moment for the strongly allowed 1Ag to 1Bu electronic excitation that is not oriented along the major axis of the polyene chain. In this paper, the experimental values of this off-axis angle are compared to semiempirical and ab initio theoretical predictions. The semiempirical computations are shown to be reliable and are extended to long chains (n = 20). The results are then extrapolated to the infinite chain limit. A nonzero value of 6°−11° for the infinite polyene is suggested by this extrapolation but state of the art ab initio results for a series of small polyenes yield a zero asymptotic value.

Series (mathematics)Ab initioExtrapolationPolyeneMolecular physicsMolecular electronic transitionchemistry.chemical_compoundDipolechemistryChain (algebraic topology)Physics::Atomic PhysicsLimit (mathematics)Physics::Chemical PhysicsPhysical and Theoretical ChemistryThe Journal of Physical Chemistry A
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ChemInform Abstract: High Electrical Conductance of Single Molecules: A Challenge in the Series of Conjugated Oligomers

2009

En route to molecular electronics: As extended, conjugated oligomers are desirable for molecular electronics, their electrical conductance should display a low attenuation factor. Zinc-complexed oligo(ethynyleneporphyrindiylethynylene)s have been prepared that are distinguished by ultralow attenuation factors in single-molecule conductance.

Series (mathematics)Electrical resistance and conductanceChemical physicsChemistryAttenuationAttenuation factorMolecular electronicsMoleculeConductanceGeneral MedicineConjugated systemChemInform
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Signal processing and frequency-dependent associative memory based on nanoswitches

2008

A signal processing concept based on nanoscale switches whose conductance can be tuned by an external stimulus between two (ON and OFF) states is proposed and analyzed theoretically. The building block of the system is formed by a metal nanoparticle linked to two electrodes by an organic ligand and a molecular switch. When we apply an alternating potential to the system of the same frequency as the periodic variation between the ON and OFF states induced on the switch, the net charge delivered by the system exhibits a sharp resonance. This resonance can be used to process an external signal by selectively extracting the weight of the different harmonics. In addition, a frequency-dependent a…

Signal processingMolecular switchSignal processingMaterials scienceContent-addressable storage ; Molecular electronics ; Nanoelectronics ; Nanoparticles ; Signal processingContent-addressable storageMolecular electronicsNanoelectronicsUNESCO::FÍSICAGeneral Physics and AstronomyMolecular electronicsConductanceNanotechnologyContent-addressable memoryNanoelectronics:FÍSICA [UNESCO]HarmonicsNanoparticlesContent-addressable storageBiological system
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