Search results for "Polarizable Continuum Model"

showing 10 items of 31 documents

Superexchange-mediated electronic energy transfer in a model dyad

2010

On the basis of time-dependent density functional theory (TD-DFT) calculations coupled to the polarizable continuum model (PCM) and single molecule spectroscopic studies, we provide a detailed investigation of excitation energy transfer within a model bi-chromophoric system where a perylene monoimide (PMI) donor is bridged to a terrylene diimide (TDI) acceptor through a ladder-type pentaphenylene (pPh) spacer. We find that the electronic excitation on the PMI donor significantly extends over the bridge giving rise to a partial charge transfer character and inducing a approximately 3-fold increase in the electronic interaction between the chromophores, which explains the failure of the Först…

StereochemistryGeneral Physics and AstronomyChromophorePolarizable continuum modelAcceptorchemistry.chemical_compoundPartial chargechemistrySuperexchangeChemical physicsExcited stateDensity functional theoryPhysical and Theoretical ChemistryPerylenePhysical Chemistry Chemical Physics
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Lewis Acid Mediated Domino Reaction between 2-Cyclohexenone and Methyl Azide - A DFT Study

2005

We have studied the Lewis acid mediated domino reaction between 2-cyclohexenone and methyl azide at the B3LYP/6-31G* and B3LYP/6-31+G**//B3LYP/6-31G* levels of theory. A complete survey of the potential energy surface is presented, and the structures of the stationary points and the corresponding molecular mechanism are discussed. The calculations suggest that the product, a cyclopentanone derivative, is formed by means of a domino process that comprises three consecutive reactions. The first and rate-limiting step is a concerted 1,3-dipolar cycloaddition between the Lewis acid coordinated cyclohexenone and methyl azide that yields the corresponding bicyclic 1,2,3-triazoline. The second rea…

StereochemistryOrganic ChemistryCyclopentanonePolarizable continuum modelMedicinal chemistryTautomerCycloadditionchemistry.chemical_compoundchemistryCascade reactionCyclohexenoneLewis acids and basesPhysical and Theoretical ChemistryMethyl azideEuropean Journal of Organic Chemistry
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DFT study on the cycloreversion of thietane radical cations.

2011

The molecular mechanism of the cycloreversion (CR) of thietane radical cations has been analyzed in detail at the UB3LYP/6-31G* level of theory. Results have shown that the process takes place via a stepwise mechanism leading to alkenes and thiobenzophenone; alternatively, formal [4 + 2] cycloadducts are obtained. Thus, the CR of radical cations 1a, b(center dot+) is initiated by C2-C3 bond breaking, giving common intermediates INa,b. At this stage, two reaction pathways are feasible involving ion molecule complexes IMCa,b (i) or radical cations 4a,b(center dot+) (ii). Calculations support that 1a(center dot+) follows reaction pathway (leading to the formal [4 + 2] cycloadducts 5a). By cont…

ThietaneSTEADY-STATEFree RadicalsStereoisomerismOXETANEOxetanePhotochemistryPolarizable continuum modelPHOTOINDUCED-ELECTRON-TRANSFERPhotoinduced electron transferchemistry.chemical_compoundQUIMICA ORGANICACICLOREVESIONCationsMolecule(THIA)PYRYLIUM SALTSSulfhydryl CompoundsPhysical and Theoretical ChemistryDNA PHOTOLYASEDFT CALCULATIONREPAIRMolecular StructureTHIETANECLEAVAGEOtras Ciencias QuímicasCiencias QuímicasStereoisomerismRADICAL CATIONchemistryRadical ionEXCITED-STATESPOLARIZABLE CONTINUUM MODELCyclizationDENSITYQuantum TheoryThiobenzophenoneCIENCIAS NATURALES Y EXACTASThe journal of physical chemistry. A
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The lineshape of the electronic spectrum of the green fluorescent protein chromophore, part I: gas phase.

2014

The vibronic spectra of the green fluorescent protein chromophore analogues p-hydroxybenzylidene-2,3-dimethylimidazolinone (HBDI) and 3,5-tert-butyl-HBDI (35Bu) are similar in the vacuum, but very different in water or ethanol. To understand this difference, we have computed the vibrationally resolved solution spectra of these chromophores, using the polarizable continuum model (PCM) to account for solvent effects on the (harmonic) potential energy surfaces (PES). In agreement with experiment, we found that the vibrational progression increases with the polarity of the solvent, but we could neither reproduce the broadening, nor the large difference between the absorption spectra of HBDI and…

Vibrational spectroscopyComputational chemistrygenetic structuresAbsorption spectroscopySpectrophotometry InfraredPopulationGreen Fluorescent ProteinsAnalytical chemistryElectronsPolarizable continuum modelMolecular physicsAbsorptionMolecular dynamicsBenzyl CompoundsVibronic spectroscopyGreen fluorescent proteinPhysical and Theoretical ChemistryeducationImidazolinesta116education.field_of_studyChemistryTemperatureChromophoreChromophoresPotential energyAtomic and Molecular Physics and OpticsQuantum TheoryThermodynamicsGasesSolvent effectsChemphyschem : a European journal of chemical physics and physical chemistry
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The triplet excited state of the biocative compound thiabendazole. Characterization and suitability as reporter for cyclodextrin complexation

2012

Fluorescence spectroscopy, laser flash photolysis (LPF), and density functional theory calculations have been performed to characterize the photobehavior of thiabendazole (1). Direct LFP of 1 results in the generation of a transient absorbing at λmax = 570 nm identified as the triplet excited state (31∗). The intersystem crossing quantum yield is 0.91, and the triplet energy is 288 kJ mol−1. The singlet–triplet energy gap is 84 kJ mol−1. The behavior of thiabendazole within CDs results in a marked enhancement of the triplet lifetime, this change is attributed to the mobility restrictions of included 1 imposed by the cyclodextrin cavities.

chemistry.chemical_classificationOptimizationCyclodextrinBeta-CyclodextrinGeneral Physics and AstronomyQuantum yieldHuman-SerumDensityProteinsPhotochemistryPolarizable continuum modelBenzimidazoleFluorescence spectroscopyIntersystem crossingQUIMICA ORGANICAchemistryExcited stateSolventTransitionFlash photolysisPolarizable continuum modelDensity functional theoryPhysical and Theoretical ChemistryApproximation
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Reaction Mechanism of an Intramolecular Oxime Transfer Reaction: A Computational Study

2014

Density functional theory (PBE0/def2-TZVPP) calculations in conjunction with a polarizable continuum model were used to assess the mechanism of the intramolecular oxime transfer reaction that leads to the formation of isoxazolines. Different diastereomers of the intermediates as well as different oximes (formaldehyde and acetone oxime) were considered. The computed reaction profile predicts the water-addition and -expulsion steps as the highest barriers along the pathway, a conclusion that is in line with the experimental evidence obtained previously for these reactions.

chemistry.chemical_compoundReaction mechanismchemistryIntramolecular forceOrganic ChemistryDiastereomerFormaldehydeDensity functional theoryPhotochemistryOximeta116Polarizable continuum modelAcetone oximeThe Journal of Organic Chemistry
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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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Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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Reaction Mechanism of an Intramolecular Oxime Transfer Reaction: A Computational Study

2014

Density functional theory (PBE0/def2-TZVPP) calculations in conjunction with a polarizable continuum model were used to assess the mechanism of the intramolecular oxime transfer reaction that leads to the formation of isoxazolines. Different diastereomers of the intermediates as well as different oximes (formaldehyde and acetone oxime) were considered. The computed reaction profile predicts the water-addition and -expulsion steps as the highest barriers along the pathway, a conclusion that is in line with the experimental evidence obtained previously for these reactions. peerReviewed

polarizable continuum modeldensity-functional theory
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A Theoretical and Experimental Investigation of the Spectroscopic Properties of a DNA-Intercalator Salphen-Type ZnIIComplex

2014

The photophysical and DNA-binding properties of the cationic zinc(II) complex of 5-triethylammonium methyl salicylidene ortho-phenylenediiminato (ZnL 2 + ) were investi- gated by a combination of experimental and theoretical methods. DFT calculations were performed on both the ground and the first excited states of ZnL 2 + and on its possi- ble mono- and dioxidation products, both in vacuo and in selected solvents mimicked by the polarizable continuum model. Comparison of the calculated absorption and fluores- cence transitions with the corresponding experimental data led to the conclusion that visible light induces a two-elec- tron photooxidation process located on the phenylenediimi- nato…

spectroscopyNO ligandStereochemistryIntercalation (chemistry)Ionic bondingmetal complex Fluorescence spectroscopy DNA recognition metal complexes organometallics complex formation DNA binding drugs fluorescence spectroscopy equilibrium constants reaction mechanisms nucleic acids affinity binding mode thermodynamics speciationmetal complexesbinding modePhenylenediaminesPolarizable continuum modelCatalysisdrugsmetal complexthermodynamicsintercalationcomplex formationOrganometallic CompoundsA-DNADNA bindingFluorescence spectroscopyDNA recognitionphotochemistryLigandChemistrySpectrum AnalysisphotooxidationOrganic ChemistryCationic polymerizationequilibrium constantsGeneral Chemistrydensity functional calculationFluorescenceZincCrystallographyreaction mechanismsnucleic acidsspeciationSettore CHIM/03 - Chimica Generale E InorganicaExcited stateaffinityfluorescenceorganometallics
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