Search results for " Quantum"

showing 10 items of 3215 documents

Vibrational analysis of the electronic spectrum of ethylene based onab initio SCF-CI calculations

1972

Ab initio calculations for CH2 twisting and CC stretching vibrational wavefunctions and energy levels are reported for various electronic states of ethylene C2H4. Electronic transition moments between these states are also obtained to allow a calculation of the oscillator strengths for vibrational transitions involved in various electronic band systems; from this study it is concluded that thevertical electronic energy differenceΔE e may differ significantly from the energy of the absorption maximumΔE max with which it is often equated. In particular it is found in the case of theπ→π * singlet-singlet excitation of ethylene that theΔE e value overestimates the most probable vibrational tran…

ChemistryTransition dipole momentAb initioMolecular electronic transitionsymbols.namesakeAb initio quantum chemistry methodsRydberg formulasymbolsChiropracticsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsAbsorption (electromagnetic radiation)Wave functionExcitationTheoretica Chimica Acta
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General occurrence of polar twisted minima in the ionic singlet excited surfaces of polyenes

1982

Except for a few cases, the lowest closed shell SCF solutions for the twisted geometries of polyenes involves delocalized nonpolarized MO’s, and represents a meaningless mixture of radicalar gound state and ionic excited states. Higher (quasi) solutions allow a realistic approach of the polarized ionic states. Orthogonality to the radicalar ground state may be imposed without important loss of energy. Further extensive CI does not modify significantly the situation. These statements are illustrated through ab initio calculations of butadiene and hexatriene. This approach allows us to show that slight distortions stablize polar minima even in ’’homosymmetric’’ molecules such as all‐trans hex…

ChemistryUNESCO::FÍSICAGeneral Physics and AstronomyIonic bondingElectronic structurePolyenesExcited StatesSelf−Consistent FieldDelocalized electronElectronic StructureAb initio quantum chemistry methods:FÍSICA [UNESCO]Polyenes ; Self−Consistent Field ; Electronic Structure ; Excited StatesExcited statePhysics::Atomic and Molecular ClustersSinglet statePhysical and Theoretical ChemistryAtomic physicsPhysics::Chemical PhysicsGround stateOpen shell
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Semiconducting Clathrates Meet Gas Hydrates: Xe24[Sn136]

2014

Semiconducting Group 14 clathrates are inorganic host–guest materials with a close structural relationship to gas hydrates. Here we utilize this inherent structural relationship to derive a new class of porous semiconductor materials: noble gas filled Group 14 clathrates (Ngx[M136], Ng=Ar, Kr, Xe and M=Si, Ge, Sn). We have carried out high-level quantum chemical studies using periodic Local-MP2 (LMP2) and dispersion-corrected density functional methods (DFT-B3LYP-D3) to properly describe the dispersive host–guest interactions. The adsorption of noble gas atoms within clathrate-II framework turned out to be energetically clearly favorable for several host–guest systems. For the energetically…

Chemistrybusiness.industryOrganic ChemistryClathrate hydrateeducationNoble gasGeneral ChemistryCatalysisSemiconductorAdsorptionChemical physicsComputational chemistryAb initio quantum chemistry methodsAtomNoble gas configurationbusinessPorosityta116
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Classical and quantum aspects of electric-magnetic duality rotations in curved spacetimes

2018

It is well known that the source-free Maxwell equations are invariant under electric-magnetic duality rotations, $\mathrm{F}\ensuremath{\rightarrow}\mathrm{F}\mathrm{cos}\ensuremath{\theta}+^{\ensuremath{\star}}\mathrm{F}\mathrm{sin}\ensuremath{\theta}$. These transformations are indeed a symmetry of the theory in the Noether sense. The associated constant of motion is the difference in the intensity between self-dual and anti-self-dual components of the electromagnetic field or, equivalently, the difference between the right and left circularly polarized components. This conservation law holds even if the electromagnetic field interacts with an arbitrary classical gravitational background.…

Chiral anomalyElectromagnetic fieldPhysicsConservation lawConstant of motion010308 nuclear & particles physicsFOS: Physical sciencesGeneral Relativity and Quantum Cosmology (gr-qc)Quantum Hall effect01 natural sciencesGeneral Relativity and Quantum CosmologyGravitationsymbols.namesakeMaxwell's equations0103 physical sciencessymbolsNoether's theorem010306 general physicsMathematical physics
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CHIRAL ANOMALY IN ASHTEKAR'S APPROACH TO CANONICAL GRAVITY

1998

The Dirac equation in Riemann–Cartan spacetimes with torsion is reconsidered. As is well-known, only the axial covector torsion A, a one-form, couples to massive Dirac fields. Using diagrammatic techniques, we show that besides the familiar Riemannian term only the Pontrjagin type four-form dA ∧ dA does arise additionally in the chiral anomaly, but not the Nieh–Yan term d* A, as has been claimed recently. Implications for cosmic strings in Einstein–Cartan theory as well as for Ashtekar's canonical approach to quantum gravity are discussed.

Chiral anomalyPhysicsGravity (chemistry)Dirac (software)Astronomy and AstrophysicsType (model theory)Cosmic stringGeneral Relativity and Quantum Cosmologysymbols.namesakeClassical mechanicsSpace and Planetary ScienceDirac equationTorsion (algebra)symbolsQuantum gravityMathematical PhysicsMathematical physicsInternational Journal of Modern Physics D
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Process-independent strong running coupling

2016

We unify two widely different approaches to understanding the infrared behaviour of quantum chromodynamics (QCD), one essentially phenomenological, based on data, and the other computational, realised via quantum field equations in the continuum theory. Using the latter, we explain and calculate a process-independent running-coupling for QCD, a new type of effective charge that is an analogue of the Gell-Mann--Low effective coupling in quantum electrodynamics. The result is almost identical to the process-dependent effective charge defined via the Bjorken sum rule, which provides one of the most basic constraints on our knowledge of nucleon spin structure. This reveals the Bjorken sum to be…

Chiral perturbation theoryNuclear TheoryFOS: Physical sciences01 natural sciencesEffective nuclear chargeNuclear Theory (nucl-th)High Energy Physics - LatticeHigh Energy Physics - Phenomenology (hep-ph)Quantum mechanics0103 physical sciencesBeta function (physics)Quantum field theoryNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentPhysicsCoupling constantQuantum chromodynamics010308 nuclear & particles physicsHigh Energy Physics - Lattice (hep-lat)High Energy Physics::PhenomenologyHigh Energy Physics - PhenomenologySum rule in quantum mechanicsUltraviolet fixed pointProcess-independentRunning coupling
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Ionization Energies of ClO and Cl2O2

1996

The ionization energies of chlorine oxide (ClO) and its dimer (Cl2O2) have been measured using monochromatic synchrotron radiation in the 10−20 eV energy regime in combination with photoionization mass spectrometry. The threshold energy of ClO+ (m/z = 51) is found at 10.85 ± 0.05 eV, whereas the ionization threshold of Cl2O2+ (m/z = 102) occurs at 11.05 ± 0.05 eV. The experimental values are compared to results from ab initio calculations, where three stable isomers of Cl2O2 are considered:  dichlorine peroxide (ClOOCl), chloryl chloride (ClClO2), and chlorine chlorite (ClOClO). The results indicate that the experimental threshold energy of Cl2O2+ is due to adiabatic ionization of ClOOCl. T…

Chlorine oxideChemistryAb initio quantum chemistry methodsIonizationGeneral EngineeringAnalytical chemistryAppearance energyPhotoionizationPhysical and Theoretical ChemistryIonization energyThreshold energyMass spectrometryThe Journal of Physical Chemistry
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Ab initio calculations and vibrational spectroscopy on the phenylenediamine isomers

1998

Molecular orbital calculations at HF and MP2 levels have been performed using the 6-3IG** basis set for full geometry optimization of the phenylenediamine isomers. Our results show that only a transoid conformer is found for o-phenylenediamine, whereas cis and trans conformers exist for m- and p-phenylenediamine. Vibrational normal modes have been also analyzed for the gas phase and in chloroform solution, and compared with experimental data we have obtained using FTIR spectroscopy. © 1998 Elsevier Science B.V.

ChloroformChemistryInfrared spectroscopyCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryPhysical chemistryFTIR spectroscopy Geometry optimization Vibrational mode analysisMolecular orbitalPhysical and Theoretical ChemistryFourier transform infrared spectroscopyConformational isomerismCis–trans isomerismBasis set
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Tautomeric preferences of phthalones and related compounds

2007

Abstract Multinuclear magnetic resonance and IR spectra prove that although 2-(diacylmethyl)pyridines and 2-(diacylmethyl)quinolines are β-diketones, their proton transfer product present in chloroform solution is not ketoenol but enaminone (earlier opinions were contradictory). Quinoline derivatives are less zwitterionic by character than the respective pyridyl congeners. The β-diketone form itself may also be rarely present in the solution. X-ray data show that 2-(2(1H)-pyridinylidene)-1H-indene-1,3(2H)-dione, i.e., enaminone tautomer of 2-(pyridin-2-yl)-2H-indene-1,3-dione, is also the only form present in crystal. Ab initio calculations show that the enaminone is usually more stable tha…

ChloroformProtonOrganic ChemistryQuinolineInfrared spectroscopyAromaticityBiochemistryTautomerchemistry.chemical_compoundchemistryAb initio quantum chemistry methodsComputational chemistryDrug DiscoveryMoleculeTetrahedron
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(1Z,3Z)-3-[Quinolin-2(1H)-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol: An unexpected most stable tautomer of 1,3-bis(quinolin-2-yl)acetone

2009

Abstract 1 H, 13 C and 15 N NMR spectra reveal that CDCl 3 solution of 1,3-bis(quinolin-2-yl)acetone contains only ( 1Z , 3Z )-3-[quinolin-2(1 H )-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol. The proton transfer takes place between two basic centers of the molecule, which means that the process is an identity reaction by character. The situation is completely different from that detected in chloroform solution of 1,3-bis(pyridin-2-yl)acetone where three different tautomers are in equilibrium with each other. Although the proton transfers in both ( 1Z , 3Z )-3-[quinolin-2(1 H )-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol and ( 1Z , 3Z )-3-hydroxy-1-[quinolin-2(1 H )-ylidene-4-quinolin-2-yl]but-3-e…

ChloroformStereochemistryChemical shiftOrganic ChemistryConjugated systemTautomerMedicinal chemistryAnalytical ChemistryInorganic ChemistryNMR spectra databasechemistry.chemical_compoundchemistryAb initio quantum chemistry methodsAcetoneMoleculeSpectroscopyJournal of Molecular Structure
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