Search results for "electron transfer"

showing 10 items of 282 documents

Photo Induced Radical Reactions

2012

This article discusses a number of reactions of potential synthetic interest occurring through photochemically generated organic radicals. Emphasis is placed on the nature of the resulting photoproducts, whose formation is discussed on a mechanistic basis. If available, experimental evidence (obtained by laser flash photolysis or related time-resolved techniques) is provided. The material is organized according to the reaction types, for instance, homolytic cleavage, mesolytic cleavage, radical addition, and oxidative or reductive electron transfer. In addition to the classical carboncarbon or carbonhydrogen bond breaking processes, such as the Norrish type I reaction, the hydrogen abstract…

Type I reactionElectron transferChemistryRadicalFlash photolysisBond breakingCleavage (embryo)PhotochemistryHydrogen atom abstractionBond cleavage
researchProduct

Ab initio calculations of the transfer parameters and coulombic repulsion and estimation of their effects on the electron delocalization and magnetic…

2003

International audience; In this work, we present ab initio calculations on embedded fragments that permit to extract the value of the effective electron transfer integral and coulombic repulsion between W nearest neighbour atoms in a mixed-valence αPW12O40 Keggin polyoxoanion. This allows us to perform a quantitative study of the influence of these two parameters on the magnetic properties of Keggin polyoxoanions reduced by two electrons. We surprisingly find that the electron transfer between edge-sharing and corner-sharing WO6 octahedra have very close values, and show that the punctual charges estimation of coulombic repulsion may not be accurate enough to study the electronic distributi…

Valence (chemistry)010405 organic chemistryChemistryElectron010402 general chemistry01 natural sciencesInductive couplingMolecular physics0104 chemical sciencesIonInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryElectron transfersymbols.namesakeAb initio quantum chemistry methodsMaterials ChemistrysymbolsDiamagnetismPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)
researchProduct

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
researchProduct

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)
researchProduct

Mixed-Valence Molecular Unit for Quantum Cellular Automata: Beyond the Born-Oppenheimer Paradigm through the Symmetry-Assisted Vibronic Approach.

2016

In this article, we focus on the electron-vibrational problem of the tetrameric mixed-valence (MV) complexes proposed for implementation as four-dot molecular quantum cellular automata (mQCA).1 Although the adiabatic approximation explored in ref 2 is an appropriate tool for the qualitative analysis of the basic characteristics of mQCA, like vibronic trapping of the electrons encoding binary information and cell-cell response, it loses its accuracy providing moderate vibronic coupling and fails in the description of the discrete pattern of the vibronic levels. Therefore, a precise solution of the quantum-mechanical vibronic problem is of primary importance for the evaluation of the shapes o…

Valence (chemistry)ChemistryBorn–Oppenheimer approximation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesComputer Science ApplicationsAdiabatic theoremElectron transferVibronic couplingsymbols.namesakeQuantum mechanicsPhysics::Atomic and Molecular ClusterssymbolsVibronic spectroscopyPhysics::Chemical PhysicsPhysical and Theoretical Chemistry0210 nano-technologyQuantumQuantum cellular automatonJournal of chemical theory and computation
researchProduct

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
researchProduct

Magnetic mixed-valence d2-d1-d1 trimers with partial electron delocalization: vibronic coupling and magnetic properties

1993

Abstract The energy levels and magnetic properties of a triangular mixed-valence cluster d1-d1-d2 with electron delocalization in a pair of sites are examined from a model that takes into account electron transfer, magnetic exchange, and vibronic coupling. We show that the electron transfer process involves besides the usual double-exchange parameter, and additional parameter referred to as exchange transfer. This last parameter accounts for the interaction between the moving electron of the mixed valence pair and the electron localized in the third side. We notice that the role of double exchange is to stabilize a ferromagnetic alignment of the spins on the mixed-valence pair. A comparison…

Valence (chemistry)Condensed matter physicsSpin statesChemistryGeneral Physics and AstronomyElectronDelocalized electronElectron transferVibronic couplingFerromagnetismPhysics::Atomic and Molecular ClustersAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryChemical Physics
researchProduct

A Deficiency in Respiratory Complex I in Heart Mitochondria from Vitamin A-Deficient Rats Is Counteracted by an Increase in Coenzyme Q

1997

Defects of NADH:coenzyme Q oxidoreductase (complex I) of mitochondria have been described in many congenital and acquired diseases. Administration of coenzyme Q (CoQ, ubiquinone) has been shown to benefit patients with some of these diseases. However, the mechanisms by which CoQ exerts the therapeutic effects are not clearly understood. A reason could be the lack of saturation of CoQ, in kinetic terms, for complex I activity. However, this hypothesis has not been proved in vivo because of the difficulty to incorporate CoQ into the mitochondrial membranes. We have found a deficiency in respiratory complex I in heart mitochondria from vitamin A-deficient rats which was accompanied by high CoQ…

Vitaminmedicine.medical_specialtyAcquired diseasesUbiquinoneBiophysicsMitochondrionBiologyBiochemistryMitochondria Heartchemistry.chemical_compoundRespiratory Complex IOxidoreductaseInternal medicinemedicineAnimalsNADH NADPH OxidoreductasesMolecular Biologychemistry.chemical_classificationElectron Transport Complex IVitamin A Deficiencyfood and beveragesCell BiologyRatsElectron transfer rateKineticsEndocrinologychemistryCoenzyme Q – cytochrome c reductaseBiochemical and Biophysical Research Communications
researchProduct

Efficient Hot Electron Transfer in Quantum Dot-Sensitized Mesoporous Oxides at Room Temperature

2018

Hot carrier cooling processes represent one of the major efficiency losses in solar energy conversion. Losses associated with cooling can in principle be circumvented if hot carrier extraction toward selective contacts is faster than hot carrier cooling in the absorber (in so-called hot carrier solar cells). Previous work has demonstrated the possibility of hot electron extraction in quantum dot (QD)-sensitized systems, in particular, at low temperatures. Here we demonstrate a room-temperature hot electron transfer (HET) with up to unity quantum efficiency in strongly coupled PbS quantum dot-sensitized mesoporous SnO2. We show that the HET efficiency is determined by a kinetic competition b…

Work (thermodynamics)Materials scienceBioengineeringHot electron transfer02 engineering and technologyPhoton energy010402 general chemistryKinetic energyterahertz spectroscopy01 natural sciencesquantum dot-sensitized solar cellsstrong couplingGeneral Materials ScienceSDG 7 - Affordable and Clean Energy/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energybusiness.industryMechanical EngineeringPbS quantum dotsGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesTerahertz spectroscopy and technologyQuantum dotOptoelectronicsQuantum efficiencyAstrophysics::Earth and Planetary Astrophysics0210 nano-technologybusinessMesoporous materialExcitationNano Letters
researchProduct

Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyri…

2016

We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(…

XantphosLigand02 engineering and technologyGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences22'-Bipyridine0104 chemical scienceschemistry.chemical_compoundCrystallographyElectron transferchemistryExcited stateMaterials ChemistrySinglet state0210 nano-technology
researchProduct