Search results for "Fer"

showing 10 items of 33109 documents

Multi-scale multireference configuration interaction calculations for large systems using localized orbitals: Partition in zones

2012

A new multireference configuration interaction method using localised orbitals is proposed, in which a molecular system is divided into regions of unequal importance. The advantage of dealing with local orbitals, i.e., the possibility to neglect long range interaction is enhanced. Indeed, while in the zone of the molecule where the important phenomena occur, the interaction cut off may be as small as necessary to get relevant results, in the most part of the system it can be taken rather large, so that results of good quality may be obtained at a lower cost. The method is tested on several systems. In one of them, the definition of the various regions is not based on topological considerati…

010304 chemical physicsChemistryGeneral Physics and AstronomyMultireference configuration interactionMolecular orbital theory010402 general chemistry01 natural sciences0104 chemical sciencesLinear combination of atomic orbitalsMulti-configurational self-consistent field0103 physical sciencesMolecular orbitalComplete active spaceStatistical physicsPhysical and Theoretical ChemistryAtomic physicsBasis setNatural bond orbital
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Effect of molecular Stokes shift on polariton dynamics

2021

When the enhanced electromagnetic field of a confined light mode interacts with photoactive molecules, the system can be driven into the regime of strong coupling, where new hybrid light-matter states, polaritons, are formed. Polaritons, manifested by the Rabi split in the dispersion, have shown potential for controlling the chemistry of the coupled molecules. Here, we show by angle-resolved steady-state experiments accompanied by multi-scale molecular dynamics simulations that the molecular Stokes shift plays a significant role in the relaxation of polaritons formed by organic molecules embedded in a polymer matrix within metallic Fabry-Pérot cavities. Our results suggest that in the case …

010304 chemical physicsScatteringRelaxation (NMR)Physics::OpticsGeneral Physics and Astronomy010402 general chemistry7. Clean energy01 natural sciencesMolecular physics0104 chemical sciencessymbols.namesakeMolecular dynamicsMolecular vibrationStokes shift0103 physical sciencesPolaritonsymbolsRadiative transferPhysical and Theoretical ChemistryExcitationThe Journal of Chemical Physics
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High Gradient Performance of an S-Band Backward Traveling Wave Accelerating Structure for Medical Hadron Therapy Accelerators

2018

The high-gradient performance of an accelerating structure prototype for a medical proton linac is presented. The structure was designed and built using technology developed by the CLIC collaboration and the target application is the TULIP (Turning Linac for Proton therapy) proposal developed by the TERA foundation. The special feature of this design is to produce gradient of more than 50 MV /m in low-β accelerating structures (v/c=0.38). The structure was tested in an S-band test stand at CERN. During the tests, the structure reached over above 60 MV/m at 1.2 μs pulse length and breakdown rate of about 5x10⁻⁶ bpp. The results presented include ultimate performance, long term behaviour and …

010308 nuclear & particles physicsU01 Medical Applications[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]08 Applications of Accelerators Tech Transfer and Industrial RelationscavityAccelerators and Storage Rings01 natural sciencesAccelerator Physicsradiation0103 physical scienceslinac010306 general physicsaccelerating-gradientproton
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Oxidovanadium(V) amine bisphenolates as epoxidation, sulfoxidation and catechol oxidation catalysts

2017

Air-stable oxidovanadium(V) complexes with tetradentate amine bisphenolate ligands were made by the reaction of VOSO4·xH2O and ligand precursors in MeOH solutions. Isolated compounds were studied as catechol oxidase models as well as catalysts for epoxidation and sulfoxidation reactions. All compounds can catalyse such oxidation reactions without notable structure-activity correlations. The 51V NMR studies indicate that the complexes turn to the number of different species during the catalytic experiments. peerReviewed

010402 general chemistry01 natural sciencesRedoxvanadiiniCatalysisInorganic ChemistryTurn (biochemistry)chemistry.chemical_compoundMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryCatechol oxidaseta216ta116Catecholbiologycatalysis010405 organic chemistryLigandoxo transferbiomimetic0104 chemical scienceschemistrykatalyysibiology.proteinvanadiumAmine gas treatingInorganic Chemistry Communications
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Unveiling the Occurrence of Co(III) in NiCo Layered Electroactive Hydroxides: The Role of Distorted Environments

2020

Co- and Ni-based layered hydroxides constitute a unique class of two-dimensional inorganic materials with exceptional chemical diversity, physicochemical properties and outstanding performance as supercapacitors and overall water splitting catalysts. Recently, the occurrence of Co(III) in these phases has been proposed as a key factor that enhance their electrochemical performance. However, the origin of this centers and control over its contents remains as an open question. We employed the Epoxide Route to synthesize a whole set of α-NiCo layered hydroxides. The PXRD and XAS characterization alert about the occurrence of Co(III) as a consequence of the increment in the Ni content. DFT+U si…

010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysisCatalysis//purl.org/becyt/ford/1 [https]symbols.namesake//purl.org/becyt/ford/1.4 [https]LAYERED HYDROXIDESX-ray absorption spectroscopy2D MATERIALS010405 organic chemistryChemistryOrganic ChemistryFermi levelGeneral Chemistry0104 chemical sciencesCharacterization (materials science)Chemical engineeringOctahedronWATER SPLITTINGsymbolsWater splittingENERGY STORAGESUPERCAPACITANCEChemistry – A European Journal
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Switching and redox isomerism in first-row transition metal complexes containing redox active Schiff base ligands.

2014

International audience; The reversible redox isomerisms in first row transition metal complexes of the type ML2 were studied. The six ML2 complexes (M = Mn(III) (), Fe(II) (), Co(III) (), Ni(II) (), Cu(II) () and Zn(II) ()) were synthesized with a redox active Schiff base ligand [2-(3,5-di-tert-butyl-2-hydroxyphenylamino)-4-chlorophenol] (H3L) presenting different oxidation states from -2 to 0 (L(2-), L(-) and L(0)). EPR spectra and magnetic susceptibility measurements indicate the presence of complexes of the type [Mn(III)(L(2-))(L(-))] () with S = 1/2, [Fe(II)(L(-))2] () with S = 2, [Co(III)(L(2-))(L(-))] () with S = 1/2, [Ni(II)(L(-))2] () with S = 1, [Cu(II)(L(-))2] () with S = 1/2 and …

010402 general chemistryLigands01 natural sciencesRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundElectron transferTransition metalIsomerismlawCoordination ComplexesMetals HeavyElectron paramagnetic resonanceSchiff BasesValence (chemistry)Schiff base010405 organic chemistryLigand[CHIM.MATE]Chemical Sciences/Material chemistryTautomer0104 chemical sciences3. Good healthCrystallographychemistryOxidation-Reduction
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The first example of cofacial bis(dipyrrins)

2016

International audience; Two series of cofacial bis(dipyrrins) were prepared and their photophysical properties as well as their bimolecular fluorescence quenching with C-60 were investigated. DFT and TDDFT computations were also performed as a modeling tool to address the nature of the fluorescence state and the possible inter-chromophore interactions. Clearly, there is no evidence for such interactions and the bimolecular quenching of fluorescence, in comparison with mono-dipyrrins, indicates that C-60-bis(dipyrrin) contacts occur from the outside of the "mouth" of the cofacial structure.

010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisTransition metalexcitation-energiesmolecular-orbital methodsorganometallic compoundsMaterials Chemistry[CHIM]Chemical Sciencessinglet energy transfersdensity-functional theoryvalence basis-setsGroup 2 organometallic chemistryQuenching (fluorescence)010405 organic chemistryChemistryGeneral ChemistryTime-dependent density functional theorytransition-metalsFluorescence0104 chemical scienceslight-harvesting systems2nd-row elementsDensity functional theoryextended basis-sets
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Gold(II) Porphyrins in Photoinduced Electron Transfer Reactions

2019

Chemistry - a European journal 25(23), 5940 - 5949 (2019). doi:10.1002/chem.201900050

010405 organic chemistryArylOrganic ChemistryPhotoredox catalysisGeneral Chemistry010402 general chemistryPhotochemistry54001 natural sciencesRedoxPorphyrinCatalysisPhotoinduced electron transfer0104 chemical scienceslaw.inventionchemistry.chemical_compoundElectron transferchemistrylawddc:540AzideElectron paramagnetic resonance
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Two bimetallic layered materials with “Cu4Fe3” defective cubane units: syntheses, structures and magnetic properties of {[CuII(tn)]2[FeII(CN)6]}3·[Na…

2005

Abstract Reactions of the [Fe III (CN) 6 ] 3− anion with the [Cu II (tn)] 2+ ion (tn = 1,3-diaminopropane) afford the compounds {[Cu II (tn)] 2 [Fe II (CN) 6 ]}3·[Na 3 Fe III (CN) 6 ]·12H 2 O (1) and {[Cu n (tn)] 2 [Fe II (CN) 6 ]}·KCl·5H 2 O (2). Despite the differences concerning their asymmetric units, both structures present strong similar features: in both structures, the Cu(II) ion presents a square-base pyramidal CuN 5 environment and each [Fe II (CN) 6 ] 4− anion is linked to six Cu(II) ions through its six N atoms leading to infinite [Cu II (tn)] 2 [Fe II (CN) 6 ] layers which can be viewed as 2-D layered arrangement generated by the defective cubane units Cu 4 Fe 3 involving Fe-CN…

010405 organic chemistryChemistryCoordination polymerMechanical EngineeringInorganic chemistryMetals and AlloysCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsParamagnetismchemistry.chemical_compoundCrystallographyTransition metalMechanics of MaterialsCubaneMaterials ChemistryMoleculeAntiferromagnetismBimetallic stripSynthetic Metals
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Cover Picture: Dynamic Chemical Devices: Photoinduced Electron Transfer and Its Ion-Triggered Switching in Nanomechanical Butterfly-Type Bis(porphyri…

2006

010405 organic chemistryChemistryEnergy transferOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrinCatalysisPhotoinduced electron transfer0104 chemical sciencesIonElectron transferchemistry.chemical_compoundCover (algebra)Chemistry - A European Journal
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