Search results for "EXTENDED BASIS-SETS"

showing 5 items of 5 documents

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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Cation Environment of BaCeO3−Based Protonic Conductors II: New Computational Models

2011

Quantum chemical calculations have been carried out to simulate Y-doped BaCeO(3) derivatives. Hartree-Fock energy functional was used to study octahedral site environments embedded in a Pmcn orthorhombic framework, showing local arrangement characterized by Ce-O-Ce, Ce-O-Y, and Y-O-Y (Z-O-Ξ) configurations and including or not hydrogen close to the moieties encompassing those configurations. The latter are, in fact, representative of - and, in our modeling approach, were treated as - local arrangements that could be found in Y:BaCeO(3)-doped materials. The geometrical optimizations performed on the structural models and a detailed orbital analysis of these systems allowed us to confirm and …

Phase transitionExtended X-ray absorption fine structureHydrogenShell (structure)2ND-ROW ELEMENTSchemistry.chemical_elementDOPED BARIUM CERATECrystal structureEXTENDED BASIS-SETSRELATIVISTIC EFFECTIVE POTENTIALSSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)MOLECULAR-ORBITAL METHODSchemistryOctahedronSettore CHIM/03 - Chimica Generale E InorganicaComputational chemistryChemical physicsPEROVSKITE OXIDESCRYSTAL-STRUCTURESPHASE-TRANSITIONSOrthorhombic crystal systemAB-INITIO PSEUDOPOTENTIALSPhysical and Theoretical ChemistryVALENCE BASIS-SETSEnergy functionalThe Journal of Physical Chemistry A
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Random Structural Modification of a Low-Band-Gap BODIPY-Based Polymer

2017

International audience; A BODIPY thiophene polymer modified by extending conjugation of the BODIPY chromophore is reported. This modification induces tunability of energy levels and therefore absorption wavelengths in order to target lower energies.

Materials scienceBand gapthin-film transistors02 engineering and technology010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural scienceschemistry.chemical_compoundmolecular-orbital methodsorganometallic compounds[CHIM]Chemical SciencesPhysical and Theoretical Chemistrydensity-functional theoryAbsorption (electromagnetic radiation)valence basis-setsdistyryl-boradiazaindaceneschemistry.chemical_classificationPolymer modifiedfield-effect transistorspi-conjugated copolymers[CHIM.MATE]Chemical Sciences/Material chemistryPolymerChromophore021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWavelengthsolar-cellsGeneral Energychemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryextended basis-setsBODIPY0210 nano-technologyThe Journal of Physical Chemistry C
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Excited State N−H Tautomer Selectivity in the Singlet Energy Transfer of a Zinc(II)-Porphyrin-Truxene-Corrole Assembly

2017

International audience; An original corrole-containing polyad for S-1 energy transfer, in which one zinc(II)-porphyrin donor is linked to two free-base corrole acceptors by a truxene linker, is reported. This polyad exhibits a rapid zinc(II)-porphyrin*free-base corrole transfer (4.83x10(10)s(-1); 298K), even faster than the tautomerization in the excited state processes taking advantage of the good electronic communication provided by the truxene bridge. Importantly, the energy transfer process shows approximately 3-fold selectivity for one corrole N-H tautomer over the other even at low temperature (77K). This selectivity is due to the difference in the J-integral being effective in both t…

chemistry.chemical_elementDexter energy transferZinccore-modified corroles010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesmain-group elements[ CHIM ] Chemical SciencesCatalysisfree-base corroleschemistry.chemical_compoundmolecular-orbital methods[CHIM]Chemical SciencesSinglet stateCorrolecorrolesdensity-functional theoryvalence basis-setsphotophysical propertiestautomerization010405 organic chemistrytruxenesensitized solar-cellsOrganic ChemistryGeneral ChemistryTautomerPorphyrin0104 chemical scienceschemistrymesosubstituted corrolesExcited stateFRETextended basis-setsSelectivityLinker
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Metal Dependence on the Bidirectionality and Reversibility of the Singlet Energy Transfer in Artificial Special Pair-Containing Dyads

2017

International audience; The demetalation of a precursor dyad, 3, built upon a zinc(II)-containing artificial special pair and free-base antenna, leads to a new dyad, 4, for singlet energy transfer composed of cofacial free-base porphyrins (acceptor), [Fb](2) bridged by a 1,4-C6H4 group to a free-base antenna (donor), [Fb]. This dyad exhibits the general structure [M](2)-C6H4-[Fb], where [M](2) = [Fh](2), and completes a series reported earlier, where [M](2) = [Mg](2) (2) and [Zn](2) (3). The latter dyads exhibit a bidirectional energy-transfer process at 298 K for 2 and at 77 K for 3. Interestingly, a very scarce case of cycling process is observed for the zinc-containing dyad at 298 K. The…

cofacial bisporphyrin dyadsStereochemistryEnergy transferchemistry.chemical_elementZinc[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesphotoinduced electron-transferInorganic ChemistryMetalmolecular-orbital methodsMolecular orbitalSinglet statePhysical and Theoretical Chemistryphotosynthetic reaction-centerdensity-functional theoryvalence basis-setsbase hybrid diporphyrins010405 organic chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryResonance (chemistry)Acceptor0104 chemical sciencesCrystallographychemistrylight-harvesting systemsvisual_artpolarizable continuum modelvisual_art.visual_art_mediumDensity functional theoryextended basis-sets
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