Search results for "Physics::Chemical Physics"

showing 10 items of 517 documents

Ultrafast myoglobin structural dynamics observed with an X-ray free-electron laser.

2014

Light absorption can trigger biologically relevant protein conformational changes. The light-induced structural rearrangement at the level of a photoexcited chromophore is known to occur in the femtosecond timescale and is expected to propagate through the protein as a quake-like intramolecular motion. Here we report direct experimental evidence of such ‘proteinquake’ observed in myoglobin through femtosecond X-ray solution scattering measurements performed at the Linac Coherent Light Source X-ray free-electron laser. An ultrafast increase of myoglobin radius of gyration occurs within 1 picosecond and is followed by a delayed protein expansion. As the system approaches equilibrium it underg…

Biologia Strutturale[PHYS]Physics [physics]Quantitative Biology::BiomoleculesPhotolysisTime FactorsLight[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry Molecular Biology/Structural Biology [q-bio.BM]BiofisicaMyoglobinProtein ConformationLasers[PHYS.PHYS.PHYS-BIO-PH]Physics [physics]/Physics [physics]/Biological Physics [physics.bio-ph]Dinamica delle ProteineMolecular Dynamics SimulationCrystallography X-RayBiological sciences Biochemistry BiophysicsSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Article[PHYS.PHYS.PHYS-GEN-PH]Physics [physics]/Physics [physics]/General Physics [physics.gen-ph][SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsAnimalsHorsessense organsPhysics::Chemical Physics
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2,5-Dimethyl-4′-nitrobiphenyl

2006

The title compound, C14H13NO2, is a non-planar biphenyl derivative, in which the dihedral angle between the benzene rings is 62.65 (5) °.

Biphenylchemistry.chemical_compoundchemistryPolymer chemistryGeneral Materials ScienceGeneral ChemistryPhysics::Chemical PhysicsDihedral angleCondensed Matter PhysicsBenzene4-NitrobiphenylDerivative (chemistry)Acta Crystallographica Section E Structure Reports Online
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Structural symmetry breaking in octupolar tetrastyrylpyrazines and their dipole moments in equilibrium ground and Franck-Condon excited state

2018

Abstract From electrooptical absorption measurements (EOAM) follows that the dipole moment of octupolar tetrastyrylpyrazines in the equilibrium ground state is large and that the change of dipole moments upon transition to the excited Franck–Condon state is significant. Obtained results unambiguously testify to structural symmetry breaking in the studied octupolar tetrastyrylpyrazines. Molecular mechanics and semi-empirical calculations evidence that tetrastyrylpyrazines have non-planar configurations. The non-planar geometry of the molecules causes large μg values and significant change of dipole moment Δaμ after excitation. Due to large μg and Δaμ values the maxima of the first absorption…

Bond dipole momentCondensed matter physicsChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics0104 chemical sciencessymbols.namesakeDipoleAbsorption bandExcited statesymbolsSymmetry breakingPhysics::Chemical Physicsvan der Waals force0210 nano-technologyGround stateJournal of Photochemistry and Photobiology A: Chemistry
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Dipole Moment Surface of the van der Waals Complex CH4–N2

2010

The interaction-induced dipole moment surface of the van der Waals CH(4)-N(2) complex has been calculated for a broad range of intermolecular separations R and configurations in the approximation of the rigid interacting molecules at the MP2 and CCSD(T) levels of theory using the correlation-consistent aug-cc-pVTZ basis set with the basis set superposition error correction. The simple model to account for the exchange effects in the range of small overlap of the electron shells of interacting molecules and the induction and dispersion interactions for large R has been suggested. This model allows describing the dipole moment of van der Waals complexes in analytical form both for large R, wh…

Bond dipole momentNitrogenSurface Properties[PHYS.ASTR.EP]Physics [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP]Transition dipole momentVan der Waals surface[SDU.ASTR.EP]Sciences of the Universe [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP]General Physics and Astronomy[SDU.ASTR.EP] Sciences of the Universe [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP]010402 general chemistry01 natural sciencessymbols.namesake0103 physical sciencesVan der Waals radiusPhysics::Chemical PhysicsPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010304 chemical physicsChemistryIntermolecular forceVan der Waals strain[ SDU.ASTR.EP ] Sciences of the Universe [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP]0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryDipole[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry[PHYS.ASTR.EP] Physics [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP][ PHYS.ASTR.EP ] Physics [physics]/Astrophysics [astro-ph]/Earth and Planetary Astrophysics [astro-ph.EP][ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbolsQuantum Theoryvan der Waals forceAtomic physicsHydrophobic and Hydrophilic InteractionsMethane
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Equation-of-motion coupled-cluster methods for ionized states with an approximate treatment of triple excitations.

2005

The accuracy of geometries and harmonic vibrational frequencies is evaluated for two equation-of-motion ionization potential coupled-cluster methods including CC3 and CCSDT-3 triples corrections. The first two Sigma states and first Pi state of the N2 +, CO+, CN, and BO diatomic radicals are studied. The calculations show a tendency for the CC3 variant to overestimate the bond lengths and to underestimate the vibrational frequencies, while the CCSDT-3 variant seems to be more reliable. It is also demonstrated that the accuracy of such methods is comparable to sophisticated traditional multireference approaches and the full configuration interaction method.

Bond lengthCoupled clusterChemistryIonizationHarmonicGeneral Physics and AstronomyEquations of motionPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsIonization energyFull configuration interactionDiatomic moleculeThe Journal of chemical physics
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Alternative single-reference coupled cluster approaches for multireference problems: the simpler, the better.

2011

We report a general implementation of alternative formulations of single-reference coupled cluster theory (extended, unitary, and variational) with arbitrary-order truncation of the cluster operator. These methods are applied to compute the energy of Ne and the equilibrium properties of HF and C(2). Potential energy curves for the dissociation of HF and the BeH(2) model computed with the extended, variational, and unitary coupled cluster approaches are compared to those obtained from the multireference coupled cluster approach of Mukherjee et al. [J. Chem. Phys. 110, 6171 (1999)] and the internally contracted multireference coupled cluster approach [F. A. Evangelista and J. Gauss, J. Chem. …

Bond lengthCoupled clusterChemistryQuantum mechanicsMolecular vibrationGaussAnharmonicityGeneral Physics and AstronomyPhysics::Chemical PhysicsPhysical and Theoretical ChemistryUnitary statePotential energyFermi Gamma-ray Space TelescopeThe Journal of chemical physics
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Breather Molecular Complexes in a Passively Mode‐Locked Fiber Laser

2021

International audience; Breathing solitons are nonlinear waves in which the energy concentrates in a localized and oscillatory fashion. Similarly to stationary solitons, breathers in dissipative systems can form stable bound states displaying molecule-like dynamics, which are frequently called breather molecules. So far, the experimental observation of optical breather molecules and the real-time detection of their dynamics are limited to diatomic molecules, that is, bound states of only two breathers. In this work, the observation of different types of breather complexes in a mode-locked fiber laser: multibreather molecules, and molecular complexes originating from the binding of two breat…

BreatherFOS: Physical sciences02 engineering and technology01 natural sciencesMolecular physics010309 opticsFiber laser0103 physical sciencesBound statePhysics::Chemical PhysicsNonlinear Sciences::Pattern Formation and SolitonsPhysics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Intermolecular force021001 nanoscience & nanotechnologyCondensed Matter PhysicsDiatomic moleculeAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsNonlinear Sciences::Exactly Solvable and Integrable SystemsMode-lockingDissipative systemSoliton0210 nano-technologyPhysics - OpticsOptics (physics.optics)
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Potential models for the simulation of methane adsorption on graphene: development and CCSD(T) benchmarks

2018

Different force fields for the graphene–CH4 system are proposed including pseudo-atom and full atomistic models. Furthermore, different charge schemes are tested to evaluate the electrostatic interaction for the CH4 dimer. The interaction parameters are optimized by fitting to interaction energies at the DFT level, which were themselves benchmarked against CCSD(T) calculations. The potentials obtained with both the pseudo-atom and full atomistic approaches describe accurately enough the average interaction in the methane dimer as well as in the graphene–methane system. Moreover, the atom–atom potentials also correctly provide the energies associated with different orientations of the molecu…

CCSD calculationsPotential modelsUNESCO::QUÍMICADimerGeneral Physics and AstronomyThermodynamics02 engineering and technology010402 general chemistry:QUÍMICA [UNESCO]7. Clean energy01 natural sciencesStability (probability)MethaneCCSD calculations Potential models methane adsorptionlaw.inventionchemistry.chemical_compoundlawPhysics::Atomic and Molecular ClustersMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryBond energymethane adsorptionCondensed Matter::Quantum GasesPhysicsGrapheneCharge (physics)Interaction energy021001 nanoscience & nanotechnology0104 chemical scienceschemistry0210 nano-technologyPhysical Chemistry Chemical Physics
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Quantum Effects and Phase Transitions in Adsorbed Molecular Layers

1998

Phase transitions in adsorbed (two dimensional) fluids and in adsorbed layers of molecules are studied with a combination of path integral Monte Carlo (PIMC), Gibbs ensemble Monte Carlo (GEMC) and finite size scaling techniques. Entropy driven phase transitions in systems with purely repulsive interactions are analyzed as well phase diagrams of fluids with internal quantum states. Adsorbed layers of H 2 molecules at a full monolayer coverage in the \(\sqrt 3 \times \sqrt 3 \) structure have a higher transition temperature to the disordered phase compared to the system with the heavier D 2 molecules, this effect is analyzed by PIMC. Linear N 2 molecules adsorbed on graphite show a transition…

Canonical ensemblePhase transitionMaterials scienceMean field theoryTricritical pointQuantum mechanicsPhase (matter)MonolayerPhysics::Chemical PhysicsPath integral Monte CarloPhase diagram
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Intrinsic Acidity of Surface Sites in Calcium Silicate Hydrates and Its Implication to Their Electrokinetic Properties

2014

Calcium Silicate Hydrates (C–S–H) are the major hydration products of portland cement paste. The accurate description of acid–base reactions at the surface of C–S–H particles is essential for both understanding the ion sorption equilibrium in cement and prediction of mechanical properties of the hardened cement paste. Ab initio molecular dynamics simulations at the density functional level of theory were applied to calculate intrinsic acidity constants (pKa’s) of the relevant ≡SiOH and ≡CaOH2 groups on the C–S–H surfaces using a thermodynamic integration technique. Ion sorption equilibrium in C–S–H was modeled applying ab initio calculated pKa’s in titrating Grand Canonical Monte Carlo simu…

CementQuantitative Biology::BiomoleculesChemistryAb initioThermodynamicsThermodynamic integrationSorptionElectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionElectrokinetic phenomenachemistry.chemical_compoundPortland cementGeneral EnergylawCalcium silicate550 Earth sciences & geologyPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryPhysics::Chemical PhysicsComputingMilieux_MISCELLANEOUS
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