Search results for "isomers"

showing 10 items of 64 documents

BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics

2015

This work describes new anticancer agents that could be detected by optical imaging, namely optical theranostics.After a first chapter describing the context of cancer imaging and therapy, a second chapter describes a first series of BODIPY-phosphine-gold theranostics, the synthesis of which has been optimized (less steps, shortening the reaction time, scale up). Their conjugation with biomolecules (glucose, peptide) has been achieved by developing a simple and efficient method that leads to the coupling between the gold atom of the probe and the thiol of the biomolecule (modified or not), leading to a gold sulfur bound. Hence, it makes the biovectorization of the probes possible in order t…

Phosphine-GoldPhotoacoustiqueThéranostiqueProche infra-rougeIn vitro studiesÉtudes in vitroOptical ImagingPhosphine-orPhotoacousticAtropoisomèresAtropisomersAggregationNear-infraredTheranosticImagerie optiqueBODIPY[CHIM.OTHE] Chemical Sciences/OtherAgrégationPicket FencePicket-Fence
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Carborane-stilbene dyads: influence of substituents and cluster isomers on the photoluminescence properties

2017

Two novel styrene-containing meta-carborane derivatives substituted at the second carbon cluster atom (Cc) with either a methyl (Me), or a phenyl (Ph) group, are introduced herein alongside with a new set of stilbene-containing ortho- (o-) and meta- (m-) carborane dyads. The latter set of compounds has been prepared from styrenecontaining carborane derivatives via Heck coupling reaction. High regioselectivity has been achieved for these compounds by using a combination of palladium complexes [Pd2(dba)3]/[Pd(t-Bu3P)2] as a catalytic system, yielding exclusively E isomers. All compounds have been fully characterized and the crystal structures of seven of them analyzed by X-ray diffraction. Th…

PhotoluminescenceAbsorption spectroscopy010405 organic chemistryStereochemistryChemistrySubstituentRegioselectivityQuantum yield010402 general chemistry01 natural sciencesFluorescence spectroscopy0104 chemical sciencesInorganic Chemistrycluster isomersCrystallographychemistry.chemical_compoundsubstituentsHeck reactionphotoluminescence propertiesCarboranecarborane-stilbene dyadsta116
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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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Mass spectrometry and decay spectroscopy of isomers across the Z=82 shell closure

2013

Recent results from a measurement campaign studying the isomerism in neutron-deficient Tl isotopes are presented. The measurements make use of a nuclear spectroscopy setup coupled to the high-resolution Penning-trap mass spectrometer ISOLTRAP at CERN's radioactive ion-beam facility ISOLDE. The mass values of 190,194Tl are improved and a mass-spin-state assignment is carried out. An additional mass measurement of the grandparent nuclide 198At allows the deduction of the spin-state ordering in 190Tl. As a result, the excitation energies of the isomers in both Tl isotopes are determined for the first time to Eex(194Tl)=260(15) keV and E ex(190Tl)=89(12) keV. Furthermore, this allows anchoring …

PhysicsNuclear and High Energy Physics[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]010308 nuclear & particles physicsClosure (topology)Shell (structure)ISOLTRAPMass spectrometry01 natural sciencesIon trappingISOLTRAPPenning ion trapTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITY0103 physical sciencesisomersddc:530Atomic physicsNuclear Experiment010306 general physicsSpectroscopyZ=82mass spectrometry
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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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Nuclear size isomers

2016

Developing of methods of measuring the radii of nuclei in their highly excited states led to observation of those with dimensions enhanced and, probably, diminished in comparison with the corresponding ground states. Experimental data including very recent ones demonstrating that such “size isomers” belong to two groups: excited states having neutron halos (in 13C, 11Be and 9 Be) and some specific cluster states (in 12C, 13C and 11B), are discussed. peerReviewed

Physicsta114nuclear sizeExcited statePhysicsQC1-999Cluster (physics)isomersNeutronHaloAstrophysicsEngineering physicsEPJ Web of Conferences
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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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13C NMR of carbonyl compounds. 3. Structure and dynamics of protonated enones and dienones

1984

Abstract The unsaturated ketones 1 1 – 10 10 were protonated at low temperatures and studied by dynamic 13C NMR spectroscopy. Four interconverting stereoisomers were detected which differ in their conformation with respect to the CO and CC (enone) single bond.

StereochemistryOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyCarbon-13 NMRBiochemistrychemistry.chemical_compound13c nmr spectroscopychemistryComputational chemistryNMR spectroscopy of stereoisomersDrug DiscoverySingle bondEnoneTetrahedron Letters
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Electronic structure and energy decomposition analyses as a tool to interpret the redox potential ranking of naphtho-, biphenyl- and biphenylenequino…

2016

By calling on modelling approaches we have performed a comparative study on the redox properties of various naphtho-, biphenyl- and biphenylene-quinone isomers. These different compounds exhibit as a whole a redox potential range between 2.09 and 2.90 V vs. Li+/Li. A specific methodology was used to decrypt the interplay among isomerism, aromaticity and antiaromaticity modifications and the stabilization/destabilization effects due to other molecular components on this key electrochemical feature for electrode materials of batteries. In particular, energy decomposition analysis, within the Quantum Theory of Atoms in Molecules, along with the electron and electron spin population changes upo…

StereochemistryPopulationRedox potentialsGeneral Physics and Astronomy02 engineering and technologyElectronic structure010402 general chemistry01 natural sciencesRedoxLihium batteriesDFTModellingBiphenylIsomerschemistry.chemical_compoundComputational chemistryPhysical and Theoretical Chemistryeducationeducation.field_of_studyChemistryBiphenyleneAtoms in moleculesAromaticityBiphenylene021001 nanoscience & nanotechnology0104 chemical sciencesQuinoneQuantum Theory of Atoms in MoleculesNaphtoOrganic electrodes0210 nano-technologyAntiaromaticity
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