Search results for "Localized"

showing 10 items of 297 documents

IR fingerprints of U(VI) nitrate monoamides complexes: a joint experimental and theoretical study.

2010

Infrared spectra of 0.5 mol·L-1 uranium(VI) nitrate monoamide complexes in toluene have been recorded and compared with infrared spectra calculated by DFT. The investigated monoamides were N,N- dimethylformamide (DMF), N,N-dibutylformamide (DBF), and N,N- dicyclohexylformamide (DcHF). The validity of DFT calculations for describing uranium nitrate monoamide complexes has been confirmed as a fair agreement between experimental and calculated spectra was obtained. Furthermore, a topological analysis of the electron density has been carried out to characterize monoamide-uranium interactions. From this work, it appears that the increase of stability of uranylmonoamide complexes may be directly …

Theoretical studyElectron densityTopological analysis Engineering controlled terms: DimethylformamideInorganic chemistryDFT calculationStrontium compoundchemistry.chemical_elementInfrared spectroscopyLigand010402 general chemistryTopology01 natural sciencesElectrostatic interactionSpectral linechemistry.chemical_compoundDelocalized electronNitratePositive charge[CHIM]Chemical SciencesPhysical and Theoretical ChemistryElectron densitieInfrared spectrumSpectroscopyComputingMilieux_MISCELLANEOUSLigand molecule010405 organic chemistrySulfur compoundUraniumTolueneN N-Dimethylformamide0104 chemical sciencesStable complexe[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryOrganic solventUraniumPhysical chemistryDegree of polarizationDegree of polarizationMonoamideUranium compounds Engineering main heading: ComplexationTolueneThe journal of physical chemistry. A
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Cavités plasmoniques et nanosources optiques

2013

Optical microcavities exhibit high resonance quality, so that, they are of key interest for the design of low-threshold lasers or for achieving strong coupling regime. But, such systems support modes whose the volume remain diffraction limited.In this manuscript, we are interested in their plasmonic counterparts because they support confined modes at the sub-wavelength scale. First, we study an in-plane plasmonic cavity which is the transposition of 1D optical cavity to surface wave. We characterize the cavity by measuring the fluorescence lifetime of dye molecules deposited inside.Then, we are interested in 3-dimension mode confinement achieved by spherical metal nanoparticles. We discuss …

Time-resolved spectroscopyCavité plasmonique[SPI.OTHER]Engineering Sciences [physics]/Other[ SPI.OTHER ] Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/OtherSpontaneous emissionSpectroscopie résolue en tempsLocalized surface plasmon[ PHYS.COND.CM-GEN ] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Plasmonic cavity[PHYS.COND.CM-GEN] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other][PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Émission spontanéePlasmon de surface localisé
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Study of the dynamics of biomolecules by high speed atomic force microscopy and surface enhanced Raman spectroscopy

2015

This thesis focuses on the coupling of High–Speed Atomic Force Microscopy (HS-AFM) and Surface Enhanced Raman Spectroscopy (SERS) for biomolecule analysis. We have designed a fabrication protocol to manufacture “SERS-active” substrates. The efficacy of gold, silver and gold-silver bimetallic crystalline nanoparticle substrates were evaluated. We have investigated the impact of optical and morphological features of the substrates on Raman signal intensity by analyzing well-known samples such as bipyridine ethylene and methylene blue molecules. We took an interest in three distinct biological problematics with HS-AFM and SERS analyses. First, we have detected the chemical signature of cytochr…

Tip–Enhanced Raman Spectroscopy (TERS)Surface Enhanced Raman Spectroscopy (SERS)CellsProteinsDetergent resistant membrane domains (DRMs)ProtéinesSpectroscopie Raman exaltée de surface (SERS)Nanoparticle substratesNoroviruses (NoVs)Substrats de nanoparticulesHigh–Speed Atomic Force Microscopy (HS-AFM)Microscopie à force atomique haute-vitesse (HS-AFM)Diffusion Raman exaltée par effet de pointe (TERS)Détergent résistant membrane domaines (DRMs)Plasmons de Surface Localisé (LSP)Cellules[PHYS.PHYS] Physics [physics]/Physics [physics]Localized Surface Plasmons (LSP)
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Optical near-field distributions of surface plasmon waveguide modes

2003

International audience; Thin gold stripes, featuring various widths in the micrometer range, were microfabricated to obtain surface-plasmon guides on a glass substrate. Each metal stripe (MS) was excited by an incident surface-plasmon polariton which was itself launched on an extended thin gold film by the total internal reflection of a focused beam coming through the substrate. The optical near-field distributions of the surface-plasmon (sp) modes sustained by the stripes were then recorded using a photon scanning tunneling microscope (PSTM). For a fixed frequency of the incident light, these field distributions are found to depend on the widths of the stripes. We first provide an experime…

Total internal reflectionMaterials sciencePOLARITONbusiness.industrySurface plasmonPhysics::Optics02 engineering and technologyPROPAGATION021001 nanoscience & nanotechnology01 natural sciencesSurface plasmon polaritonRayOpticsMETAL-FILM0103 physical sciencesFINITE-WIDTHReflection (physics)[ SPI.NANO ] Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics010306 general physics0210 nano-technologybusinessRefractive indexPlasmonLocalized surface plasmon
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Trinuclear Mo3S7 clusters coordinated to dithiolate or diselenolate ligands and their use in the preparation of magnetic single component molecular c…

2008

A general route for the preparation of a series of dianionic Mo3S7 cluster complexes bearing dithiolate or diselenolate ligands, namely, [Mo3S7L3](2-) (where L = tfd (bis(trifluoromethyl)-1,2-dithiolate) (4(2-)), bdt (1,2-benzenedithiolate) (5(2-)), dmid (1,3-dithia-2-one-4,5-dithiolate) (6(2-)), and dsit (1,3-dithia-2-thione-4,5-diselenolate) (7(2-))) is reported by direct reaction of [Mo3S7Br6](2-) and (n-Bu)2Sn(dithiolate). The redox properties, molecular structure, and electronic structure (BP86/VTZP) of the 4(2-) to 7(2-) clusters have also been investigated. The HOMO orbital in all complexes is delocalized over the ligand and the Mo3S7 cluster core. Ligand contributions to the HOMO ra…

Trifluoromethyl010405 organic chemistryStereochemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryElectronic structure010402 general chemistry01 natural sciencesRedox0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyDelocalized electronAtomic orbitalchemistryCluster (physics)MoleculePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSInorganic chemistry
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Six-coordinate [CoIII(L)2]z (z = 1−, 0, 1+) complexes of an azo-appended o-aminophenolate in amidate(2−) and iminosemiquinonate π-radical (1−) redox-…

2018

Aerobic reaction of the ligand H2L1, 2-(2-phenylazo)-anilino-4,6-di-tert-butylphenol, CoCl2·6H2O and Et3N in MeOH under refluxing conditions produces, after work-up and recrystallization, black crystals of [Co(L1)2] (1). When examined by cyclic voltammetry, 1 displays in CH2Cl2 three one-electron redox responses: two oxidative, E11/2 = 0.30 V (peak-to-peak separation, ΔEp = 100 mV) and E21/2 = 1.04 V (ΔEp = 120 mV), and one reductive E1/2 = −0.27 V (ΔEp = 120 mV) vs. SCE. Consequently, 1 is chemically oxidized by 1 equiv. of [FeIII(η5-C5H5)2][PF6], affording the isolation of deep purple crystals of [Co(L1)2][PF6]·2CH2Cl2 (2), and one-electron reduction with [CoII(η5-C5H5)2] yielded bluish-b…

Valence (chemistry)010405 organic chemistryChemistryLigandCarbon-13 NMR010402 general chemistry01 natural sciencesTautomer0104 chemical scienceslaw.inventionInorganic ChemistryDelocalized electronCrystallographylawProton NMRDensity functional theoryElectron paramagnetic resonanceDalton Transactions
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Electron Delocalization and Electrostatic Repulsion at the Origin of the Strong Spin Coupling in Mixed-Valence Keggin Polyoxometalates: Ab Initio Cal…

2004

International audience; Cet article détaille une procédure générale qui associe l′évaluation de paramètres microscopiques et la prédiction de propriétés macroscopiques. Les principales interactions entre les électrons délocalisés sur des polyoxométalates à valence mixte sont extraites à partir du calcul de la spectroscopie de valence de fragments immergés dans un bain qui reproduit les principaux effets du reste du cristal sur le fragment considéré. Nous avons extrait non seulement la valeur du transfert électronique, du couplage magnétique et du paramètre de "exchange-transfer" entre ions métalliques premiers et seconds voisins, mais encore la valeur de la répulsion électrostatique entre l…

Valence (chemistry)010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryElectron010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesIon[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryDelocalized electronElectron transferComputational chemistryChemical physicsAb initio quantum chemistry methodsPolyoxometalatePhysics::Atomic and Molecular ClustersDiamagnetism
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Role of the electron transfer and magnetic exchange interactions in the magnetic properties of mixed-valence polyoxovanadate complexes.

2008

International audience; Modeling the properties of high-nuclearity, high-electron-population, mixed-valence (MV) magnetic systems remains one of the open challenges in molecular magnetism. In this work, we analyze the magnetic properties of a series of polyoxovananadate clusters of formula [V 18O 42] (12-) and [V 18O 42] (4-). The first compound is a fully localized spin cluster that contains 18 unpaired electrons located at the metal sites, while the second one is a MV cluster with 10 unpaired electrons largely delocalized over the 18 metal sites. A theoretical model that takes into account the interplay between electron transfer and magnetic exchange interactions is developed to explain t…

Valence (chemistry)010405 organic chemistryMagnetismChemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryElectron transfersymbols.namesakeDelocalized electronUnpaired electronAb initio quantum chemistry methodsCluster (physics)symbolsPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)
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A symmetry adapted approach to the dynamic Jahn-Teller problem: Application to mixed-valence polyoxometalate clusters with keggin structure

2012

In this article, we present a symmetry-adapted approach aimed to the accurate solution of the dynamic vibronic problem in large scale Jahn-Teller (JT) systems. The algorithm for the solution of the eigen-problem takes full advantage of the point symmetry arguments. The system under consideration is supposed to consist of a set of electronic levels mixed by the active JT and pseudo JT vibrational modes. Applying the successive coupling of the bosonic creation operators, we introduce the irreducible tensors that are called multivibronic operators. Action of the irreducible multivibronic operators on the vacuum state creates the vibrational symmetry adapted basis that is subjected to the Gram-…

Valence (chemistry)ChemistryJahn–Teller effectVacuum stateCondensed Matter PhysicsAtomic and Molecular Physics and OpticsDelocalized electronsymbols.namesakeMolecular vibrationQuantum mechanicsIrreducible representationsymbolsPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)QuantumInternational Journal of Quantum Chemistry
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Mixed‐valence trinuclear manganese clusters : Influence of the electronic transfer on the magnetic properties

1990

The magnetic behavior of mixed‐valence trinuclear clusters d4‐d4‐d5 is discussed on the basis of a model which takes into account valence delocalization and Heisenberg exchange. This model considers the competing effect between the electronic transfer and the localization of the extra electron due to an asymmetry of the triangular entity. The magnetic properties of the mixed‐valence oxo‐centered Mn(II)‐Mn(III)‐Mn(III) complexes formulated as Mn3O(O2CR)6L3 (R=Me, L=pyridine) are discussed on the basis of the developed model, supporting a significant intramolecular electron transfer. A comparison of these results to those previously reported by assuming a valence‐trapped model is given. Carlo…

Valence (chemistry)ChemistryMagnetic Propertiesmedia_common.quotation_subjectUNESCO::FÍSICAExchange InteractionsGeneral Physics and Astronomychemistry.chemical_elementManganeseElectronElectron TransferManganese ComplexesAsymmetryElectron transferCrystallographyDelocalized electronchemistry.chemical_compound:FÍSICA [UNESCO]Intramolecular forcePyridineMixed−Valence CompoundsAtomic ClustersAtomic physicsMixed−Valence Compounds ; Electron Transfer ; Magnetic Properties ; Atomic Clusters ; Manganese Complexes ; Exchange Interactionsmedia_common
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