Search results for " Isomers"

showing 10 items of 39 documents

Excitation levels and magic numbers of small parahydrogen clusters (N⩽40)

2008

The excitation energies of parahydrogen clusters have been systematically calculated by the diffusion Monte Carlo technique in steps of one molecule from 3 to 40 molecules. These clusters possess a very rich spectra, with angular momentum excitations arriving up to L=13 for the heavier ones. No regular pattern can be guessed in terms of the angular momenta and the size of the cluster. Clusters with N=13 and 36 are characterized by a peak in the chemical potential and a large energy gap of the first excited level, which indicate the magical character of these clusters. From the calculated excitation energies the partition function has been obtained, thus allowing for an estimate of thermal e…

PhysicsAngular momentumPartition function (statistical mechanics)Excited statesFOS: Physical sciencesGeneral Physics and AstronomyMonte Carlo methodsSpin isomers of hydrogenMolecular physicsSpectral lineUNESCO::FÍSICA::Química físicaEnergy gapMolecular clustersExcited stateChemical potential ; Energy gap ; Excited states ; Molecular clusters ; Monte Carlo methodsCluster (physics)Diffusion Monte CarloPhysics - Atomic and Molecular ClustersPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Atomic and Molecular Clusters (physics.atm-clus)Chemical potentialExcitationThe Journal of Chemical Physics
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Constant-adiabaticity ultralow magnetic field manipulations of parahydrogen-induced polarization: application to an AA'X spin system

2021

The field of magnetic resonance imaging with hyperpolarized contrast agents is rapidly expanding, and parahydrogen-induced polarization (PHIP) is emerging as an inexpensive and easy-to-implement method for generating the required hyperpolarized biomolecules. Hydrogenative PHIP delivers hyperpolarized proton spin order to a substrate via chemical addition of H2 in the spin-singlet state, but it is typically necessary to transfer the proton polarization to a heteronucleus (usually 13C) which has a longer spin lifetime. Adiabatic ultralow magnetic field manipulations can be used to induce the polarization transfer, but this is necessarily a slow process, which is undesirable since the spins co…

PhysicsField (physics)General Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologySpin isomers of hydrogenPolarization (waves)01 natural sciencesInduced polarization0104 chemical sciencesMagnetic fieldPhysics - Chemical PhysicsChemical additionProton spin crisisPhysical and Theoretical ChemistryAtomic physics0210 nano-technologySpin-½Physical Chemistry Chemical Physics
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A diffusion Monte Carlo study of small para-Hydrogen clusters

2007

Abstract An improved Monte Carlo diffusion model is used to calculate the ground state energies and chemical potentials of parahydrogen clusters of three to forty molecules, using two different p-H2-p-H2 interactions. The improvement is due to three-body correlations in the importance sampling, to the time step adjustment and to a better estimation of statistical errors. In contrast to path-integral Monte Carlo results, this method predicts no magic clusters other than that with thirteen molecules.

PhysicsPhysicsQC1-999FOS: Physical sciencesGeneral Physics and AstronomyFísica36.40.-cTime stepSpin isomers of hydrogenMolecular physicsmolecular clusterspara-hydrogen clusters67.40.db61.46.bcCluster (physics)Physics::Atomic and Molecular ClustersMoleculeDiffusion Monte CarloPhysics - Atomic and Molecular ClustersAtomic and Molecular Clusters (physics.atm-clus)Ground stateImportance samplingPath integral Monte Carlo
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Current density maps, magnetizability, and nuclear magnetic shielding tensors of bis-heteropentalenes. II. Furo-furan Isomers

2004

Magnetic susceptibility and nuclear magnetic shielding at the nuclei of bis-heteropentalenes formed by two furan units ([2,3-b], [3,2-b], [3,4-b], and [3,4-c] isomers) have been computed by several approximated techniques and a large Gaussian basis set to achieve near Hartree–Fock estimates. Ab initio models of the ring currents induced by a magnetic field normal to the molecular plane were obtained for the three isomeric systems of higher symmetry, showing that the π electrons give rise to intense diamagnetic circulation. The π currents are responsible for enhanced magnetic anisotropy and strong out-of-plane proton deshielding. The theoretical findings are used to build up a “diatropicity …

ProtonAb initioMagnetic Susceptibility ; Current Density ; Nuclear Screening ; Isomerism ; HF Calculations ; Ab Initio Calculations ; Magnetic Fields ; Magnetic Anisotropy ; Organic CompoundsGeneral Physics and AstronomyHF CalculationsMagnetic SusceptibilityMolecular physicsFuro-furan Isomers; Magnetizability and Nuclear Magnetic ShieldingFuro-furan IsomersIsomerismAb initio quantum chemistry methodsMagnetizability and Nuclear Magnetic ShieldingPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Condensed matter physicsOrganic CompoundsChemistryNuclear ScreeningMagnetic susceptibilityMagnetic AnisotropyMagnetic fieldUNESCO::FÍSICA::Química físicaMagnetic anisotropyMagnetic FieldsElectromagnetic shieldingDiamagnetismCurrent DensityAb Initio Calculations
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Binding abilities of dehydropeptides towards Cu(II) and Ni(II) ions. Impact of Z–E isomerization on metal ion binding

2002

The study on the binding ability of dehydro-tri- and tetrapeptides has shown that the alpha,beta-double bond has a critical effect on the peptide coordination to metal ions. It may affect the binding of the vicinal amide nitrogens by the electronic effect and stabilize the complex due to steric effects. The (Z) isomer is the most effective in stabilizing of the complexes formed. The presence of large side chain in the dehydroamino acid residue may also be critical for the coordination mode in the metallopeptide systems.

Steric effectsNickel(II) complexesE–Z isomersMetal ion bindingChemistryMetal ions in aqueous solutionPhotochemistryBiochemistryisomerizationInorganic ChemistryMetalCrystallographychemistry.chemical_compounddehydropeptidesAmidevisual_artSide chainvisual_art.visual_art_mediumElectronic effectCopper(II) complexesIsomerizationVicinalJournal of Inorganic Biochemistry : an interdisciplinary journal
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Toward a density functional description of liquid pH2.

2010

A finite-temperature density functional approach to describe the properties of parahydrogen in the liquid-vapor coexistence region is presented. The first proposed functional is zero-range, where the density-gradient term is adjusted so as to reproduce the surface tension of the liquid-vapor interface at low temperature. The second functional is finite-range and, while it is fitted to reproduce bulk pH2 properties only, it is shown to yield surface properties in good agreement with experiments. These functionals are used to study the surface thickness of the liquid-vapor interface, the wetting transition of parahydrogen on a planar Rb model surface, and homogeneous cavitation in bulk liquid…

Surface (mathematics)Chemical Physics (physics.chem-ph)Statistical Mechanics (cond-mat.stat-mech)Yield surfaceChemistryThermodynamicsFOS: Physical sciencesFísicaCondensed Matter - Soft Condensed MatterSpin isomers of hydrogenFunctional descriptionSurface tensionPhysics::Fluid DynamicsPlanarWetting transitionPhysics - Chemical PhysicsCavitationPhysics::Atomic and Molecular ClustersSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryCondensed Matter - Statistical MechanicsThe journal of physical chemistry. A
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Real-Time Nuclear Magnetic Resonance Detection of Fumarase Activity Using Parahydrogen-Hyperpolarized [1- 13 C]Fumarate

2019

Hyperpolarized fumarate can be used as a probe of real-time metabolism in vivo, using carbon-13 magnetic resonance imaging. Dissolution dynamic nuclear polarization is commonly used to produce hyperpolarized fumarate, but a cheaper and faster alternative is to produce hyperpolarized fumarate via PHIP (parahydrogen-induced polarization). In this work, we trans-hydrogenate [1-13C]acetylene dicarboxylate with para-enriched hydrogen using a commercially available Ru catalyst in water to produce hyperpolarized [1-13C]fumarate. We show that fumarate is produced in 89% yield, with succinate as a side product in 11% yield. The proton polarization is converted into 13C magnetization using a constant…

Time FactorsHydrogenNuclear Magnetic Resonancechemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesBiochemistryCatalysisFumarate HydrataseCatalysisMagnetizationchemistry.chemical_compoundColloid and Surface ChemistryFumaratesMoleculeCarbon IsotopesMolecular StructureFumarase activityCarbon Isotopes; Fumarate Hydratase; Fumarates; Molecular Structure; Time Factors; Nuclear Magnetic Resonance BiomolecularGeneral Chemistry0104 chemical sciencesAcetylenechemistryFumaraseBiomolecularJournal of the American Chemical Society
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Polarization transfer via field sweeping in parahydrogen-enhanced nuclear magnetic resonance.

2019

<div><br></div><div><table><tr><td>We show that in a spin system of two magnetically inequivalent protons coupled to a heteronucleus such as 13C, an adiabatic magnetic field sweep, passing through zero field, transfers proton singlet order into magnetization of the coupled heteronucleus. This effect is potentially useful in parahydrogen-enhanced nuclear magnetic resonance, and is demonstrated on singlet-hyperpolarized [1-13C]maleic acid, which is prepared via the reaction between [1-13C]acetylene dicarboxylic acid and para-enriched hydrogen gas. The magnetic field sweeps are of microtesla amplitudes, and have durations on the order of seconds. We sh…

Zero field NMRMaterials science010304 chemical physicsMaleic acidHydrogenField (physics)ProtonGeneral Physics and Astronomychemistry.chemical_element010402 general chemistryPolarization (waves)Spin isomers of hydrogen01 natural sciences0104 chemical sciencesMagnetic fieldchemistry.chemical_compoundMagnetizationNuclear magnetic resonancechemistry0103 physical sciencesSinglet statePhysical and Theoretical ChemistryThe Journal of chemical physics
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Decay and Fission Hindrance of Two- and Four-Quasiparticle K Isomers in 254Rf

2015

International audience; Two isomers decaying by electromagnetic transitions with half-lives of 4.7(1.1) and 247(73) mu s have been discovered in the heavy (254)Rf nucleus. The observation of the shorter-lived isomer was made possible by a novel application of a digital data acquisition system. The isomers were interpreted as the K-pi = 8(-), nu(2)(7/2(+)[624]; 9/2(-)[734]) two-quasineutron and the K-pi = 16(+), 8(-)nu(2)(7/2(+)[624]; 9/2(-)[734] circle times 8(-)pi(2) (7/2(-)[514]; 9/2(+)[624]) four-quasiparticle configurations, respectively. Surprisingly, the lifetime of the two-quasiparticle isomer is more than 4 orders of magnitude shorter than what has been observed for analogous isomer…

[PHYS]Physics [physics]General PhysicsNO-254nuclear isomersEngineeringNUCLEISTATESPhysical Sciencesrutherfordium[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]FM-250Mathematical Sciences
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Properties and interactions – melting point of tri­bromo­benzene isomers

2021

The melting points of tri­bromo­benzene isomers are correlated with the number, nature and distribution of intermolecular interactions in their structures.

chemistry.chemical_classificationHalogen bondtribromobenzene isomersChemistryIntermolecular forcemelting pointMetals and AlloysClose-packing of equal spheresResearch PapersAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCrystalmolecular symmetryCrystallographynoncovalent interactionsMaterials ChemistryMelting pointMolecular symmetrystructure-property relationshipNon-covalent interactionsMoleculehalogen bondActa Crystallographica Section B-Structural Science Crystal Engineering and Materials
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