Search results for "Atomic electron transition"

showing 10 items of 57 documents

Absorption spectrum of the and electronic transitions of ReF6

1999

Abstract The absorption spectra of the near-infrared and ultraviolet bands of ReF6 have been recorded with a commercial spectrophotometer. The vibronic assignments previously published by different authors are critically revised. A non-perturbative method has been used to calculate the linear Jahn–Teller levels for the ν5 mode in the ground electronic state. Some new vibronic parameter values are derived. The ν5 linear Jahn–Teller parameter in the X G′ g electronic state is found to be D5=0.103(9). The ultraviolet absorption spectrum has enabled us to determine relatively accurate values of the crystal-field (10Dq) and spin-orbit (ζd) parameters.

Absorption spectroscopyRhenium hexafluoridemedicine.disease_causeAtomic and Molecular Physics and OpticsUltraviolet absorption spectrumAnalytical Chemistrychemistry.chemical_compoundchemistryAtomic electron transitionmedicineVibronic spectroscopyCondensed Matter::Strongly Correlated ElectronsAtomic physicsInstrumentationSpectroscopyUltravioletSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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A Theoretical Study of the Low-Lying Excited States of trans- and cis-Urocanic Acid

1999

A multiconfigurational second-order perturbation theory (CASPT2) study of the lowest lying states in the gas-phase electronic spectra of trans- and cis-urocanic acid is presented. Geometries of both isomers have been optimized at the MP2/6-31G(d) and π-CASSCF/ANO-L(4s3p1d,2s) levels of theory. The geometries are found to differ considerably between the two levels. The vertical and 0−0 excitation spectra were calculated for each isomer. Both singlet and triplet states are described for each, including the lowest lying ππ* excitations and the nOπ* excitations. Remarkably, in the trans spectrum, it is found that the nOπ* state has a higher vertical excitation energy than the lowest ππ* (5.12 v…

Atomic electron transitionChemistryExcited stateExcitation spectraCis-Urocanic AcidSinglet statePhysical and Theoretical ChemistryPerturbation theoryAtomic physicsExcitationSpectral lineThe Journal of Physical Chemistry A
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The electronic spectrum of pyrrole

1999

The electronic spectrum of pyrrole has been investigated by performing calculations using a hierarchy of coupled-cluster models consisting of CCS, CC2, CCSD, and CC3. Basis-set effects have been investigated by carrying out calculations using correlation-consistent basis sets augmented with functions especially designed for the description of Rydberg states. Oscillator strengths, excited state dipole moments, and second moments of the electronic charge distributions have been used to characterize the electronic transitions and final states. Structures and vibrational frequencies have been calculated for a few selected states, and the importance of distinguishing between vertical and adiabat…

Basis (linear algebra)ChemistrySpectrum (functional analysis)General Physics and AstronomyElementary chargeDipolesymbols.namesakeAtomic electron transitionExcited stateRydberg formulasymbolsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processThe Journal of Chemical Physics
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Thermo‐optical investigations of NaNbO 3 thin films by spectral ellipsometry

2009

In this work a spectroscopic ellipsometry was applied to the thermo-optical investigations of sodium niobate NaNbO3 (NN) thin films at the wide temperature range of 5–820 K. The temperature dependence of complex refractive index dispersions and optical bang energy of the direct allowed electron transitions were evaluated. Additionally dynamic scans of the main ellipsometric angles at the several fixed wave lengths of 300, 400, 500 and 635 nm were performed to acquire more detailed temperature dependences of the refractive index and extinction coefficient. Pronounced minima/maxima and substantial jumps in the temperature dependence of complex refractive index and band gap energy were found a…

ChemistryBand gapAnalytical chemistryPhysics::OpticsAtmospheric temperature rangeMolar absorptivityCondensed Matter PhysicsMolecular physicsEllipsometryAtomic electron transitionvisual_artvisual_art.visual_art_mediumCeramicThin filmRefractive indexphysica status solidi c
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Theoretical study of the derivative hydrocarbons of biphenylene. I. Electronic spectrum of the biphenylene

1969

The electronic spectrum of biphenylene has been studied theoretically. The investigation is based on the semi-empirical LCAO SCF MO method with various degrees of approximations. The results have been analysed with regard to the following two factors: (a) The difference in effective electronegativity between the carbon atoms in the four-membered ring and the other carbon atoms in the molecule. (b) The inclusion of doubly excited configurations in the description of the π-electronic molecular states. The theory satisfactorily interprets the excitation energies and the nature of the electronic transitions. The predictions are particularly affected by the inclusion of the doubly excited config…

ChemistryBiphenyleneCondensed Matter PhysicsRing (chemistry)Atomic and Molecular Physics and OpticsElectronegativitychemistry.chemical_compoundLinear combination of atomic orbitalsAtomic electron transitionExcited stateMoleculePhysical and Theoretical ChemistryAtomic physicsExcitationInternational Journal of Quantum Chemistry
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Spectroscopic signatures of the carbon buckyonions C60@C180 and C60@C240: a dispersion-corrected DFT study

2013

We have investigated, using dispersion corrected DFT methods, the structure and the spectroscopic properties of carbon buckyonions C-60@C-180 and C-60@C-240. C-60, C-180 and C-240 showed a noticeable variation of their geometries in C-60@C-180 and C-60@C-240, upon encapsulation. Inclusion of the dispersion correction term in the calculations has a significant effect on the geometry. C-60@C-180 has a large positive interaction energy, while for C-60@C-240 a negative value is found indicating that only C-240 can easily accommodate C-60. In both cases dispersion interactions strongly contribute to the stabilization of the complexes. Vibrational frequencies, electronic transitions and NMR prope…

ChemistryDispersion Correctionfullerenes; computational chemistryAnalytical chemistryfullerenesGeneral Physics and AstronomyPositive interactioncomputational chemistryDFTEncapsulated buckyonionSpectroscopic.Atomic electron transitionChemical physicsPhysical and Theoretical ChemistrySettore CHIM/02 - Chimica Fisica
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Electro-optical and laser spectrofluorimetry study of coumarins 7 and 30: evidence for the existence of the close-lying electronic states and conform…

1997

Our experiments and calculations reveal a set of anomalous and interesting properties of coumarin 7 (CU7) and coumarin 30 (CU30) in solution. The spectral dependence of electro-optical coefficients and, consequently, dipole moments indicates that the absorption band is a superposition of several (at least two) electronic transitions. Probably, there are two close-lying π,π* singlet electronic excited states which contribute to the first absorption band. The calculations using the MM2 program show that both dyes in the ground state have two stable plane anti conformers. From time-resolved spectrofluorimetric measurements we obtained evidence for the existence of conformers in paraffin oil so…

ChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral Physics and AstronomyGeneral ChemistryMolecular physicsDipoleAtomic electron transitionAbsorption bandExcited stateSinglet stateAbsorption (chemistry)Ground stateConformational isomerismJournal of Photochemistry and Photobiology A: Chemistry
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Extension of Conjugation Leading to Bathochromic or Hypsochromic Effects in OPV Series

2004

Four OPV series 1-4 (a-d) with a terminal dialkylamino group as electron donor were prepared by Wittig-Horner reactions. To study the influence of the push-pull effect on the long-wavelength absorption, three of the four series contained terminal acceptor groups (CN, CHO, NO(2)). The length of the chromophores strongly affects the intramolecular charge transfer (ICT)-an effect which superimposes upon the extension of the conjugation. Increasing numbers n of repeat units cause an overall bathochromic shift for the purely donor-substituted series 1 a-4 a and the series 1 b-4 b with CN as weak acceptor. The two effects annihilate each other in the series 1 c-4 c with terminal CHO groups, so th…

ChemistryOrganic ChemistryElectron donorProtonationGeneral ChemistryChromophorePhotochemistryAcceptorCatalysischemistry.chemical_compoundAtomic electron transitionIntramolecular forceBathochromic shiftHypsochromic shiftChemistry - A European Journal
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Electronic, vibrational, and structural properties of a spin-crossover catecholato-iron system in the solid state: theoretical study of the electroni…

2005

As a functional model of the catechol dioxygenases, [(TPA)Fe(Cat)]BPh4 (TPA = tris(2-pyridylmethyl)amine and Cat = catecholate dianion) exhibits the purple-blue coloration indicative of some charge transfer within the ground state. In contrast to a number of high-spin bioinspired systems, it was previously shown that, in the solid state, [(TPA)Fe(Cat)]BPh4 undergoes a two-step S = 1/2 = S = 5/2 spin-crossover. Therefore, the electronic and vibrational characteristics of this compound were investigated in the solid state by UV/Vis absorption and resonance Raman spectroscopies over the temperature range of the transition. This allowed the charge-transfer transitions of the low-spin (LS) form …

ChemistryOrganic ChemistryResonanceGeneral ChemistryCrystal structureAtmospheric temperature rangeCatalysissymbols.namesakeCrystallographyAtomic electron transitionComputational chemistrySpin crossoverMössbauer spectroscopysymbolsRaman spectroscopyGround stateChemistry (Weinheim an der Bergstrasse, Germany)
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Probing the electronic state of a single coronene molecule by the emission from proximate fluorophores.

2012

We measured electronic transitions of the 2D graphene-type molecule hexa-peri-hexabenzocoronene (HBC) at the single-molecule level. The large intersystem crossing rate and long triplet state lifetime in the range of seconds are prohibitive for direct single-molecule observation. By covalently coupling fluorescent acceptor molecules (perylenecarboximide, PMI) to HBC, efficient singlet energy transfer gives rise to strong PMI fluorescence. Confocal single-molecule fluorescence microscopy with two excitation colours matching the HBC and PMI transition frequencies, respectively, was conducted. Single HBC-6PMI molecules were readily observed via the PMI emission. It was found that after selectiv…

ChromophoreFluorescenceAtomic and Molecular Physics and OpticsCoroneneFluorescence spectroscopychemistry.chemical_compoundIntersystem crossingchemistryAtomic electron transitionAstrophysics::Solar and Stellar AstrophysicsSinglet statePhysical and Theoretical ChemistryTriplet stateAtomic physicsChemphyschem : a European journal of chemical physics and physical chemistry
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