Search results for "iTED"

showing 10 items of 2408 documents

Full-dimensional control of the radiationless decay in pyrazine using the dynamic Stark effect

2014

We present a full quantum-mechanical study of the laser control of the radiationless decay between the B3u(nπ(*)) and B2u(ππ(*)) states of pyrazine using the dynamic Stark effect. In contrast to our previous study [Sala et al., J. Chem. Phys. 140, 194309 (2014)], where a four-dimensional model was used, all the 24 degrees of freedom are now included in order to test the robustness of the strategy of control. Using a vibronic coupling Hamiltonian model in a diabatic representation, the multi-layer version of the multi-configuration time-dependent Hartree method is exploited to propagate the corresponding wave packets. We still observe a trapping of the wavepacket on the B2u(ππ(*)) potential …

010304 chemical physicsChemistryWave packetDiabaticGeneral Physics and AstronomyHartree010402 general chemistry01 natural sciencesPotential energy0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryVibronic couplingsymbols.namesakeStark effectQuantum mechanicsExcited state[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry0103 physical sciencesPotential energy surfacesymbolsPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsComputingMilieux_MISCELLANEOUSThe Journal of Chemical Physics
researchProduct

Dynamic Polarizability and Higher-Order Electric Properties of Fluorene, Carbazole, and Dibenzofuran

2019

Static electric properties, from the dipole moment to the second-hyperpolarizability tensor γ, of the 3-membered, isoelectronic ring molecules, fluorene (FL), carbazole (CR), and dibenzofuran (DBF), have been calculated at various levels of approximation. The electron correlation effects have been included at the coupled-cluster (CC) level, using CCSD and CC2 versions of the method. DFT calculations with the CAM-B3LYP functional have also been performed, and the results are compared to the CC values. The electric property-tailored Pol basis set and its more compact Z3Pol version have been employed in all static calculations. Differences between dipole polarizability values computed at the P…

010304 chemical physicsElectronic correlationChemistryCarbazoleFluorene010402 general chemistry01 natural sciencesMolecular physics0104 chemical scienceschemistry.chemical_compoundDipolePolarizabilityExcited state0103 physical sciencesPhysical and Theoretical ChemistryBasis setExcitationJournal of Physical Chemistry A
researchProduct

Steering the excited state dynamics of a photoactive yellow protein chromophore analogue with external electric fields

2014

Abstract The first excited state of the Photoactive Yellow Protein chromophore exhibits a strong charge transfer character and the dipole moments of the excited and ground states differ significantly. Furthermore, the excited state charge distribution changes during the isomerization of this chromophore. These observations suggest that external electric fields can be used to control photo-isomerization, providing a new concept for developing photochromic devices, such as e-paper or optical memory. To test this idea, we performed excited state dynamics simulations and static calculations of a PYP chromophore analogue (pCK − ) in an external electric field. By adjusting direction and strength…

010304 chemical physicsField (physics)ChemistryCharge densitySurface hoppingChromophore010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesBiochemistryMolecular physics0104 chemical sciencesPhotochromismDipoleElectric fieldExcited state0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical Chemistryta116ComputingMilieux_MISCELLANEOUS
researchProduct

Dynamics of the excited-state hydrogen transfer in a (dG)·(dC) homopolymer: intrinsic photostability of DNA

2018

Multiscale molecular dynamics simulations reveal out-of-plane distortions that favour DNA photostability. A novel photostability mechanism involving four proton transfers and triggered by a nearby Na+ ion is also unveiled.

010304 chemical physicsProtonChemistryBase pairGuanineGeneral ChemistryHydrogen atom010402 general chemistry01 natural sciences0104 chemical sciencesNucleobase[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundChemistryChemical physicsExcited state0103 physical sciencesMolecule[CHIM]Chemical SciencesGround stateComputingMilieux_MISCELLANEOUS
researchProduct

Luminescent TOP Nanosensors for Simultaneously Measuring Temperature, Oxygen, and pH at a Single Excitation Wavelength

2019

Two nanosensors for simultaneous optical measurements of the bioanalytically and biologically relevant analytes temperature (“T”), oxygen (“O”), and pH (“P”) have been designed. These “TOP” nanosensors are based on 100 nm-sized silica-coated polystyrene nanoparticles (PS-NPs) doped with a near-infrared emissive oxygen- and temperature-sensitive chromium(III) complex ([Cr(ddpd)2][BPh4]3, CrBPh4) and an inert reference dye (Nile Red, NR or 5,10,15,20-tetrakis(pentafluorophenyl) porphyrin, TFPP) and are covalently labeled with pH-sensitive fluorescein isothiocyanate (FITC). These emitters can be excited at the same wavelength and reveal spectrally distinguishable emission bands, allowing for r…

010401 analytical chemistryDopingAnalytical chemistryNile redNanoparticle010402 general chemistry01 natural sciencesPorphyrinFluorescence0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryNanosensorExcited stateLuminescenceAnalytical Chemistry
researchProduct

Mechanism of activated chemiluminescence of cyclic peroxides: 1,2-dioxetanes and 1,2-dioxetanones

2017

Almost all chemiluminescent and bioluminescent reactions involve cyclic peroxides. The structure of the peroxide and reaction conditions determine the quantum efficiency of light emission. Oxidizable fluorophores, the so-called activators, react with 1,2-dioxetanones promoting the former to their first singlet excited state. This transformation is inefficient and does not occur with 1,2-dioxetanes; however, they have been used as models for the efficient firefly bioluminescence. In this work, we use the SA-CASSCF/CASPT2 method to investigate the activated chemiexcitation of the parent 1,2-dioxetane and 1,2-dioxetanone. Our findings suggest that ground state decomposition of the peroxide com…

010405 organic chemistryChemistryGeneral Physics and Astronomy010402 general chemistryPhotochemistrySupermolecule01 natural sciencesPeroxideLUCIFERIDAE0104 chemical scienceslaw.inventionchemistry.chemical_compoundlawExcited stateBioluminescenceLight emissionSinglet statePhysical and Theoretical ChemistryGround stateChemiluminescencePhysical Chemistry Chemical Physics
researchProduct

An investigation of photo- and pressure-induced effects in a pair of isostructural two-dimensional spin-crossover framework materials

2014

International audience; Two new isostructural iron(II) spin-crossover (SCO) framework (SCOF) materials of the type [Fe(dpms)2 (NCX)2 ] (dpms=4,4'-dipyridylmethyl sulfide; X=S (SCOF-6(S)), X=Se (SCOF-6(Se))) have been synthesized. The 2D framework materials consist of undulating and interpenetrated rhomboid (4,4) nets. SCOF-6(S) displays an incomplete SCO transition with only approximately 30 % conversion of high-spin (HS) to low-spin iron(II) sites over the temperature range 300-4 K (T1/2 =75 K). In contrast, the NCSe(-) analogue, SCOF-6(Se), displays a complete SCO transition (T1/2 =135 K). Photomagnetic characterizations reveal quantitative light- induced excited spin-state trapping (LIES…

010405 organic chemistryChemistryIronOrganic ChemistrySpin transitionMineralogyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryAtmospheric temperature range010402 general chemistrySpin crossover01 natural sciencesCatalysisLIESST0104 chemical sciencesCoordination polymersChalcogenCrystallographySpin crossoverExcited stateMetastabilityMagnetic propertiesChalcogensIsostructural
researchProduct

Harnessing Fluorescence versus Phosphorescence Ratio via Ancillary Ligand Fine-Tuned MLCT Contribution

2016

A series of gold(I) alkynyl-diphosphine complexes (XC6H4C2Au)PPh2—spacer—PPh2(AuC2C6H4X); spacer = —C2(C6H4)nC2— (A1, n = 2, X = CF3; A2, n = 2, X = OMe; A3, n = 3, X = CF3; A4, n = 3, X = OMe), —(C6H4)n— (B5, n = 3, X = OMe; B6, n = 4, X = OMe) were prepared, and their photophysical properties were investigated. The luminescence behavior of the titled compounds is dominated by the diphosphine spacer, which serves as an emitting ππ* chromophore. The complexes exhibit dual emission, comprising low and high energy bands of triplet (phosphorescence) and singlet (fluorescence) origins, respectively. The electron-donating characteristics of ancillary groups X significantly affect the LLCT/MLCT c…

010405 organic chemistryChemistryLigandChromophore010402 general chemistry01 natural sciencesFluorescence0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsphosphorescenceCrystallographyGeneral EnergyIntersystem crossinggold complexesExcited stateOrganic chemistryfluorescenceSinglet statePhysical and Theoretical ChemistryLuminescencePhosphorescenceta116Journal of Physical Chemistry C
researchProduct

Excited-State Kinetics of an Air-Stable Cyclometalated Iron(II) Complex.

2019

The complex class [Fe(N^N^C)(N^N^N)]+ with an Earth-abundant metal ion has been repeatedly suggested as a chromophore and potential photosensitizer on the basis of quantum chemical calculations. Synthesis and photophysical properties of the parent complex [Fe(pbpy)(tpy)]+ (Hpbpy=6-phenyl-2,2'-bipyridine and tpy=2,2':6',2''-terpyridine) of this new chromophore class are now reported. Ground-state characterization by X-ray diffraction, electrochemistry, spectroelectrochemistry, UV/Vis, and X-ray spectroscopy in combination with DFT calculations proves the high impact of the cyclometalating ligand on the electronic structure. The photophysical properties are significantly improved compared to …

010405 organic chemistryChemistryLigandOrganic ChemistryChemieGeneral ChemistryElectronic structureChromophore010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundBipyridineExcited stateTriplet stateTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

A Fully Conjugated TTF-π-TCAQ System: Synthesis, Structure, and Electronic Properties

2011

The synthesis of the first fully conjugated tetrathiafulvalene-tetracyano-p-quinodimethane ((TTF)-TCNQ)-type system has been carried out by means of a Julia-Kocienski olefination reaction. In particular, a tetracyanoanthraquinodimethane (TCAQ) formyl derivative and two new sulfonylmethyl-exTTFs (exTTF = 2-[9-(1,3-dithiol-2-ylidene)anthracen-10(9H)-ylidene]-1,3-dithiole)--prepared as new building blocks--were linked. A variety of experimental conditions reveal that the use of sodium hexamethyldisilazane (NaHMDS) as base in THF afforded the E olefins with excellent stereoselectivity. Theoretical calculations at the B3LYP/6-31G** level point to highly distorted exTTF and TCAQ that form an almo…

010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryConjugated system010402 general chemistryPhotochemistry01 natural sciencesAcceptorCatalysis0104 chemical sciencesIonchemistry.chemical_compoundRadical ionExcited stateGround stateDerivative (chemistry)TetrathiafulvaleneChemistry - A European Journal
researchProduct