Search results for "coupling [Higgs particle]"

showing 10 items of 443 documents

Simulated annealing with restrained molecular dynamics using a flexible restraint potential: Theory and evaluation with simulated NMR constraints

1996

A new functional representation of NMR-derived distance constraints, the flexible restraint potential, has been implemented in the program CONGEN (Bruccoleri RE, Karplus M, 1987, Biopolymers 26:137-168) for molecular structure generation. In addition, flat-bottomed restraint potentials for representing dihedral angle and vicinal scalar coupling constraints have been introduced into CONGEN. An effective simulated annealing (SA) protocol that combines both weight annealing and temperature annealing is described. Calculations have been performed using ideal simulated NMR constraints, in order to evaluate the use of restrained molecular dynamics (MD) with these target functions as implemented i…

Coupling constantQuantitative Biology::BiomoleculesChemistryCrambinNuclear magnetic resonance spectroscopyDihedral angleEnergy minimizationBiochemistryMolecular physicsMaxima and minimaMolecular dynamicsCrystallographySimulated annealingMolecular BiologyProtein Science
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Role of Disorder on the Dynamics of a Nonlinear Model for DNA Thermal Denaturation

1992

The dynamics of thermal denaturation of DNA is a good example in which nonlinearity coexits with disorder. The amplitude of the motions is so high that bonds break and the base sequence is inhomogeneous since it contains the genetic code. Using a simple nonlinear model, we study the role of local inhomogeneities or of extended disorder on the dynamics of the localized excitations and on the denaturation rate by numerical simulations at constrained temperature. Approximate analytical results are obtained for the trapping of the breatherlike excitations by isolated defects and the statistical mechanics of the disordered molecule.

Coupling constantQuantitative Biology::BiomoleculesNonlinear systemNucleic Acid DenaturationAmplitudeMathematical modelChemistryChemical physicsMoleculeStatistical mechanicsStatistical physicsMorse potential
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Quantum chemical calculations of formyl radicals

1975

The ground state (2 A′) of the fluoroformyl radical, FCO, has been investigated by the unrestricted Hartree-Fock method. Pulay's force method for open-shell systems has been applied to calculate the complete quadratic force field and the diagonal cubic force constants. The force relaxation method has been used to determine the equilibrium geometry of FCO: . Adjusting the diagonal force constants to the observed vibrational frequencies of 19F12C16O and taking the values for the off-diagonal force constants from the UHF calculations, the force field of FCO is found to be: . This force field is compared with experiment and with the force fields of HCO, H2CO, and F2CO. The ground state of the F…

Coupling constantQuantum chemicalChemistryRadicalDiagonalBiophysicsCondensed Matter PhysicsForce field (chemistry)IonQuadratic equationPhysical and Theoretical ChemistryAtomic physicsGround stateMolecular BiologyMolecular Physics
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Pentaquark decay width in QCD sum rules

2005

In a diquark-diquark-antiquark picture of the pentaquark we study the decay $\Theta \rightarrow K^{+} n$ within the framework of QCD sum rules. After evaluation of the relevant three-point function, we extract the coupling $g_{\Theta nK}$ which is directly related to the pentaquark width. Restricting the decay diagrams to those with color exchange between the meson-like and baryon-like clusters reduces the coupling constant by a factor of four. Whereas a small decay width might be possible for a positive parity pentaquark, it seems difficult to explain the measured width for a pentaquark with negative parity.

Coupling constantQuantum chromodynamicsPhysicsNuclear and High Energy PhysicsQCD sum rulesParticle physicsHigh Energy Physics::LatticeHigh Energy Physics::PhenomenologyHyperonFOS: Physical sciencesCoupling (probability)PentaquarkNuclear physicsHigh Energy Physics - PhenomenologyParticle decayColor modelHigh Energy Physics - Phenomenology (hep-ph)High Energy Physics::ExperimentNuclear ExperimentPhysical Review D
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Spectroscopic analysis of vibronic relaxation pathways in molecular spin qubit [Ho(W5O18)2]9−: sparse spectra are key

2021

Molecular vibrations play a key role in magnetic relaxation processes of molecular spin qubits as they couple to spin states, leading to the loss of quantum information. Direct experimental determination of vibronic coupling is crucial to understand and control the spin dynamics of these nano-objects, which represent the limit of miniaturization for quantum devices. Herein, we measure the vibrational properties of the molecular spin qubit $[$Ho(W$_5$O$_{18}$)$_2]^{9-}$ by means of magneto-infrared spectroscopy. Our results allow us to unravel the vibrational decoherence pathways in combination with $ab$ $initio$ calculations including vibronic coupling. We observe field-induced spectral cha…

Coupling constantQuantum decoherenceSpin statesCondensed Matter - Mesoscale and Nanoscale PhysicsChemistryRelaxation (NMR)FOS: Physical sciences02 engineering and technologyVibració010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics3. Good health0104 chemical sciencesInorganic ChemistryVibronic couplingQubitMesoscale and Nanoscale Physics (cond-mat.mes-hall)CristallsPhysical and Theoretical ChemistryQuantum informationPhysics::Chemical Physics0210 nano-technologySpin-½
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A statistical study of the additivity of substituent effects on the5J(HH) long-range coupling constant of the formyl proton in substituted benzaldehy…

1982

The additivity of chloro and hydroxy substituent effects on the formyl proton spin-spin coupling constants with the meta ring proton, 5J(HH), has been tested with 15 chlorinated benzaldehydes and hydroxybenzaldehydes by multiple linear regression analysis. No general additivity rule was detected with whole data. Using benzaldehyde as the reference substance, a good correlation was achieved for p-hydroxybenzaldehydes. The same reference compound was not suitable for o-hydroxy derivatives; a much better correlation was observed using o-hydroxybenzaldehyde as a reference compound in the latter case.

Coupling constantRange (particle radiation)ProtonStereochemistrySubstituentGeneral ChemistryRing (chemistry)Benzaldehydechemistry.chemical_compoundchemistryComputational chemistryAdditive functionGeneral Materials ScienceMultiple linear regression analysisOrganic Magnetic Resonance
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Global nuclear structure aspects of tensor interaction

2008

A direct fit of the isoscalar spin-orbit and both isoscalar and isovector tensor coupling constants to the f5/2-f7/2 SO splittings in 40Ca, 56Ni, and 48Ca requires: (i) a significant reduction of the standard isoscalar spin-orbit strength and (ii) strong attractive tensor coupling constants. The aim of this paper is to address the consequences of these strong attractive tensor and weak spin-orbit fields on total binding energies, two-neutron separation energies and nuclear deformability.

Coupling constantReductPhysicsNuclear and High Energy PhysicsIsovectorNuclear TheoryIsoscalarNuclear TheoryNuclear structureGeneral Physics and AstronomyFOS: Physical sciencesNuclear Theory (nucl-th)Quantum electrodynamicsTensorNuclear theory
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Prediction of water's isotropic nuclear shieldings and indirect nuclear spin–spin coupling constants (SSCCs) using correlation‐consistent and polariz…

2009

Density functional theory (DFT) was used to estimate water's isotropic nuclear shieldings and indirect nuclear spin-spin coupling constants (SSCCs) in the Kohn-Sham (KS) complete basis set (CBS) limit. Correlation-consistent cc-pVxZ and cc-pCVxZ (x = D, T, Q, 5, and 6), and their modified versions (ccJ-pVxZ, unc-ccJ-pVxZ, and aug-cc-pVTZ-J) and polarization-consistent pc-n and pcJ-n (n = 0, 1, 2, 3, and 4) basis sets were used, and the results fitted with a simple mathematical formula. The performance of over 20 studied density functionals was assessed from comparison with the experiment. The agreement between the CBS DFT-predicted isotropic shieldings, spin-spin values, and the experimenta…

Coupling constantSOPPA(CCSD)Condensed matter physicsChemistryIsotropywaterKohn–Sham equationsPropagatorspin–spin coupling constantsGeneral ChemistryPolarization (waves)DFT‐NMRnuclear isotropic shieldingsSSCCSOPPAGeneral Materials ScienceDensity functional theoryAtomic physicscomplete basis set limitSpin (physics)Basis setMagnetic Resonance in Chemistry
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Energy landscape properties studied using symbolic sequences

2006

We investigate a classical lattice system with $N$ particles. The potential energy $V$ of the scalar displacements is chosen as a $\phi ^4$ on-site potential plus interactions. Its stationary points are solutions of a coupled set of nonlinear equations. Starting with Aubry's anti-continuum limit it is easy to establish a one-to-one correspondence between the stationary points of $V$ and symbolic sequences $\bm{\sigma} = (\sigma_1,...,\sigma_N)$ with $\sigma_n=+,0,-$. We prove that this correspondence remains valid for interactions with a coupling constant $\epsilon$ below a critical value $\epsilon_c$ and that it allows the use of a ''thermodynamic'' formalism to calculate statistical prope…

Coupling constantStatistical Mechanics (cond-mat.stat-mech)FOS: Physical sciencesEnergy landscapeStatistical and Nonlinear PhysicsGeometryDisordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Disordered Systems and Neural NetworksCondensed Matter PhysicsPotential energyPower lawStationary pointSingularityGround stateCondensed Matter - Statistical MechanicsSaddleMathematical physicsMathematicsPhysica D: Nonlinear Phenomena
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13C nuclear magnetic resonance study of some phosphinolipids: Assignments and conformational studies

1989

13C chemical shifts and 31P, 13C spin-spin coupling constants are reported for six model phosphinates and eight synthetic phosphinolipids. The complex spectra of the synthetic phosphinolipids could be assigned from increments and couplings derived from the model compounds. Based on these investigations the 3J(PC) couplings of 7–15 Hz indicate a preferential trans orientation of the respective head-group carbon relative to the phosphorus. This behaviour is similar to that of natural phosphatidylcholine lipids.

Coupling constantStereochemistryChemical shiftPhospholipidchemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopySpectral lineCrystallographychemistry.chemical_compoundchemistryPhosphatidylcholineChemical solutionGeneral Materials ScienceCarbonMagnetic Resonance in Chemistry
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