Search results for "Vibronic coupling"

showing 10 items of 42 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
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Intersystem crossing in Fe(II) coordination compounds

1994

Fe(II) spin-crossover systems can be quantitatively converted from the low-spin (LS) to the high-spin (HS) state well below the thermal transition temperature by irradiating either into the metal-ligand charge transfer or d-d absorption bands, and even in low-spin systems a transient population of the HS state can be achieved. This fact can be made use of to determine HS → LS relaxation rate constants for a wide variety of Fe(II) spin-crossover and low-spin systems. The HS → LS relaxation shows strong deviations from an Arrhenius behaviour, with nearly temperature-independent tunnelling below ∼70 K and a thermally activated process above ∼100 K. The range of more than 12 orders of magnitude…

Arrhenius equationNuclear and High Energy Physicseducation.field_of_studyChemistryPopulationCondensed Matter PhysicsInternal conversion (chemistry)PhotochemistryMolecular physicsAtomic and Molecular Physics and OpticsVibronic couplingsymbols.namesakeIntersystem crossingReaction rate constantsymbolsRelaxation (physics)Physical and Theoretical ChemistryeducationQuantum tunnellingHyperfine Interactions
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FT Raman and DFT Study on a Series of All-antiOligothienoacenes End-Capped with Triisopropylsilyl Groups

2009

minal a positions. These substituents aid in purification and solution processability, and can be removed under mild chemical conditions. For the first time, we have the opportunity to analyze a series of oligothienoacenes to gain insight into the fundamental structure–property relationships with respect to the addition of each ring. Furthermore, this series of compounds can be directly compared to other well-studied series of closely related oligomers, such as nonfused oligothiophenes and fully fused all-syn oligothienoacenes. [7] To gain precise insight into relationships between the structure and properties of a wide range of p-conjugated molecular Herein, we study the p-conjugational pr…

Atomic and Molecular Physics and OpticsHomologous serieschemistry.chemical_compoundsymbols.namesakeCrystallographyVibronic couplingchemistryComputational chemistryMolecular vibrationsymbolsThiopheneMolecular orbitalPhysical and Theoretical ChemistryRaman spectroscopyHOMO/LUMORaman scatteringChemPhysChem
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Coherent Manipulation of Polarization in Mixed-Valence Compounds by Electric Pulse via Landau–Zener Transitions

2012

In this contribution, we predict and theoretically investigate the effects of the electric field pulse in mixed valence (MV) dimers. These systems exhibit bistability with a large internal dipole moment mediated by the itinerant electron trapped by the vibronic coupling. In this sense, they are similar to single molecular magnets (SMMs) that are bistable systems possessing large long-living magnetization and exhibiting Landau−Zener (LZ) transitions. We propose a scheme for a controllable LZ tunnelling in MV systems that provides also a possibility to control the dipole moment of a dimeric MV unit. It is supposed that the static electric field initially polarizes the system, and then the uni…

BistabilityCondensed matter physicsChemistryElectronMagnetostaticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMagnetizationPolarization densityDipoleVibronic couplingGeneral EnergyElectric fieldPhysical and Theoretical ChemistryAtomic physicsThe Journal of Physical Chemistry C
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Vibronic Relaxation Pathways in Molecular Spin Qubit Na9[Ho(W5O18)2]·35H2O under Pressure

2023

In order to explore how spectral sparsity and vibronic decoherence pathways can be controlled in a model qubit system with atomic clock transitions, we combined diamond anvil cell techniques with synchrotron-based far infrared spectroscopy and first-principles calculations to reveal the vibrational response of Na9[Ho(W5O18)2]·35H2O under compression. Because the hole in the phonon density of states acts to reduce the overlap between the phonons and f manifold excitations in this system, we postulated that pressure might move the HoO4 rocking, bending, and asymmetric stretching modes that couple with the MJ = ±5, ±2, and ±7 levels out of resonance, reducing their …

Chemistry (miscellaneous)strategies to minimize decoherenceMaterials Chemistryspin qubithigh pressure vibrational spectroscopyQuímicaVibracióvibronic couplingElectronic Optical and Magnetic MaterialsMagnetochemistry
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Spectroscopic analysis of vibronic relaxation pathways in molecular spin qubit [Ho(W5O18)2]9−: sparse spectra are key

2021

Molecular vibrations play a key role in magnetic relaxation processes of molecular spin qubits as they couple to spin states, leading to the loss of quantum information. Direct experimental determination of vibronic coupling is crucial to understand and control the spin dynamics of these nano-objects, which represent the limit of miniaturization for quantum devices. Herein, we measure the vibrational properties of the molecular spin qubit $[$Ho(W$_5$O$_{18}$)$_2]^{9-}$ by means of magneto-infrared spectroscopy. Our results allow us to unravel the vibrational decoherence pathways in combination with $ab$ $initio$ calculations including vibronic coupling. We observe field-induced spectral cha…

Coupling constantQuantum decoherenceSpin statesCondensed Matter - Mesoscale and Nanoscale PhysicsChemistryRelaxation (NMR)FOS: Physical sciences02 engineering and technologyVibració010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics3. Good health0104 chemical sciencesInorganic ChemistryVibronic couplingQubitMesoscale and Nanoscale Physics (cond-mat.mes-hall)CristallsPhysical and Theoretical ChemistryQuantum informationPhysics::Chemical Physics0210 nano-technologySpin-½
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Local dynamic properties of the heme pocket in native and solvent-induced molten-globule-like states of cytochrome c

2002

We report the Soret absorption band, down to cryogenic temperature, of native and molten-globule-like state of horse heart cytochrome c. The band profile is analyzed in terms of vibronic coupling of the heme normal modes to the electronic transition in the framework of the Franck-Condon approximation. From the temperature dependence of the Gaussian broadening and of the peak position, we obtain information on the 'bath' of low frequency harmonic motions of the heme group within the heme pocket. The reported data indicate that, compared to the native state, the less rigid tertiary structure of the molten globule is reflected in a higher flexibility of the heme pocket and in greater conformat…

GlycerolProtein FoldingHot TemperatureCytochromeProtein ConformationBiophysicsCytochrome c GroupHemeProtein dynamicsBiochemistrychemistry.chemical_compoundMolten-globule proteinsNative stateSettore BIO/10HemeBinding SitesbiologySpectrum AnalysisProtein dynamicsOrganic ChemistryMolten globuleOptical absorption spectroscopyCrystallographyVibronic couplingchemistryAbsorption bandbiology.proteinMolten-globule proteins; Optical absorption spectroscopy; Protein dynamicsProtein foldingMathematics
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Heme symmetry, vibronic structure, and dynamics in heme proteins: ferrous nicotinate horse myoglobin and soybean leghemoglobin.

2000

We report the visible and Soret absorption bands, down to cryogenic temperatures, of the ferrous nicotinate adducts of native and deuteroheme reconstituted horse heart myoglobin in comparison with soybean leghemoglobin-a. The band profile in the visible region is analyzed in terms of vibronic coupling of the heme normal modes to the electronic transition in the framework of the Herzberg–Teller approximation. This theoretical approach makes use of the crude Born–Oppenheimer states and therefore neglects the mixing between electronic and vibrational coordinates; however, it takes into account the vibronic nature of the visible absorption bands and allows an estimate of the vibronic side bands…

HemeproteinsHemeproteinBiophysicsHemePhotochemistryBiochemistryVibrationMolecular electronic transitionSpectral lineBiomaterialschemistry.chemical_compoundAnimalsFerrous CompoundsHorsesHemeMyoglobinProtein dynamicsOrganic ChemistryNicotinic AcidsTemperatureGeneral MedicineProtein Structure TertiaryLeghemoglobinVibronic couplingMyoglobinchemistrySpectrophotometryMolecular vibrationSoybeansBiopolymers
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Excited state decay of cyclometalated polypyridine ruthenium complexes: insight from theory and experiment.

2016

Deactivation pathways of the triplet metal-to-ligand charge transfer ((3)MLCT) excited state of cyclometalated polypyridine ruthenium complexes with [RuN5C](+) coordination are discussed on the basis of the available experimental data and a series of density functional theory calculations. Three different complex classes are considered, namely with [Ru(N^N)2(N^C)](+), [Ru(N^N^N)(N^C^N)](+) and [Ru(N^N^N)(N^N^C)](+) coordination modes. Excited state deactivation in these complex types proceeds via five distinct decay channels. Vibronic coupling of the (3)MLCT state to high-energy oscillators of the singlet ground state ((1)GS) allows tunneling to the ground state followed by vibrational rela…

Ligand field theory010405 organic chemistryChemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryVibronic couplingExcited stateVibrational energy relaxationDensity functional theorySinglet stateAtomic physicsPhosphorescenceGround stateDalton transactions (Cambridge, England : 2003)
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ChemInform Abstract: Excited State Decay of Cyclometalated Polypyridine Ruthenium Complexes: Insight from Theory and Experiment

2016

Deactivation pathways of the triplet metal-to-ligand charge transfer (3MLCT) excited state of cyclometalated polypyridine ruthenium complexes with [RuN5C]+ coordination are discussed on the basis of the available experimental data and a series of density functional theory calculations. Three different complex classes are considered, namely with [Ru(N^N)2(N^C)]+, [Ru(N^N^N)(N^C^N)]+ and [Ru(N^N^N)(N^N^C)]+ coordination modes. Excited state deactivation in these complex types proceeds via five distinct decay channels. Vibronic coupling of the 3MLCT state to high-energy oscillators of the singlet ground state (1GS) allows tunneling to the ground state followed by vibrational relaxation (path A…

Ligand field theoryVibronic couplingChemistryExcited stateVibrational energy relaxationDensity functional theoryGeneral MedicineSinglet statePhosphorescenceGround stateMolecular physicsChemInform
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