Search results for "Fermi resonance"

showing 10 items of 12 documents

Anomalous temperature dependence of the IR spectrum of polyalanine

1997

Abstract We have studied the temperature dependence of the infrared spectra of acetanilide (ACN), tryptophan–(alanine) 15 , and tyrosine–(alanine) 15 . No sidebands of the amide-I vibration were observed in the polypeptides, but two anomalous sidebands of the NH stretch with a similar temperature dependence as that of the anomalous amide-I vibrational mode at 1650 cm −1 of crystalline ACN were detected. Fermi resonance combined with the appearance of a red-shifted sideband of NH stretch through coupling to lattice modes seems to explain this band structure. Observations are indicative of excitons that may occur in polypeptides as well as in single crystals of ACN.

AlaninePhysics::Biological PhysicsQuantitative Biology::BiomoleculesSidebandChemistryExcitonGeneral Physics and AstronomyInfrared spectroscopy02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physics3. Good healthchemistry.chemical_compoundNuclear magnetic resonanceLattice (order)0103 physical sciencesFermi resonancePhysical and Theoretical Chemistry010306 general physics0210 nano-technologyElectronic band structureAcetanilideChemical Physics Letters
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Vibrational spectral studies of methyl 3-(4-methoxyphenyl)prop-2-enoate, a new organic non-linear optic crystal

2005

Single crystals of methyl 3-(4-methoxyphenyl)prop-2-enoate were grown by the slow evaporation technique and vibrational spectral analysis was carried out using near-IR Fourier transform Raman and Fourier transform IR spectroscopy. Ab initio quantum computations were also performed at the HF/6–311G (d,p) level to derive the equilibrium geometry, vibrational wavenumbers and intensities and first hyperpolarizability. The large NLO efficiency predicted for the first time in this new class of compounds was confirmed by powder efficiency experiments. Hartree–Fock calculations reveal that the endocyclic angle at the junction of the propeonate group and the phenyl ring is decreased from 120° by 2.5…

ChemistryAnalytical chemistryAb initioInfrared spectroscopyHyperpolarizabilityRing (chemistry)AcceptorCrystallographysymbols.namesakeAb initio quantum chemistry methodssymbolsGeneral Materials ScienceFermi resonancePhysics::Chemical PhysicsRaman spectroscopySpectroscopyJournal of Raman Spectroscopy
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Raman spectroscopy of acetic acid monomer and dimers isolated in solid argon

2011

Acetic acid (AA) monomer and its dimers were studied by means of Raman spectroscopy combined with the matrix isolation technique. All fundamental bands of CH3COOH monomer were identified, including the CH3 torsional mode. Additionally, three overtone or combination modes were observed as a result of their enhanced intensities by Fermi resonance (FR). Twenty bands of the cyclic dimer (C2h) were identified and assigned, among which appear all intermolecular modes. Bands due to two different higher energy forms of the dimer were also identified. The experimental assignments are supported by ab initio calculations. Copyright © 2011 John Wiley & Sons, Ltd.

ChemistryHydrogen bondOvertoneDimerMatrix isolationPhotochemistryCrystallographychemistry.chemical_compoundsymbols.namesakeMonomerAb initio quantum chemistry methodssymbolsGeneral Materials ScienceFermi resonanceRaman spectroscopyta116SpectroscopyJournal of Raman Scpectroscopy
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Raman Scattering in CuCl under Pressure

1999

Raman spectra of CuCl were measured under hydrostatic pressures up to 14 GPa at low temperatures (T = 5 K). The anomaly in the Raman lineshape of zincblende CuCl at frequencies near the transverse-optic (TO) mode, which consists of a broad structure with several maxima, disappears at a pressure near 3 GPa. This effect is well reproduced by a model calculation of the anharmonic coupling of the TO mode to acoustic two-phonon states (Fermi resonance). Alternative interpretations of the TO Raman anomaly in terms of local vibrational modes of Cu atoms in off-center positions are not supported by the present results. Raman spectra indicate the existence of the phase CuCl-IIa in a narrow pressure …

Condensed matter physicsChemistryPhononCondensed Matter PhysicsMolecular physicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials Sciencesymbols.namesakeX-ray Raman scatteringDispersion relationMolecular vibrationsymbolsCondensed Matter::Strongly Correlated ElectronsCoherent anti-Stokes Raman spectroscopyFermi resonanceRaman spectroscopyRaman scatteringphysica status solidi (b)
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High resolution CARS spectrum and analysis of the v1bandQ-branch of carbon dioxide

1988

High resolution coherent anti-Stokes Raman spectroscopy (CARS) has been applied to the study of the Q-branch of the fundamental vibrational v 1 band of CO2 in the Fermi resonance region near 1285·5 cm-1. Thanks to the use of high spectral quality (linewidth = 6 MHz) injection-locked flashlamp-pumped dye lasers, it was possible to resolve this band for the first time. The spectrum was recorded at a pressure of 5 kPa (37·5 Torr) at room temperature. We measured the line positions and collisional widths for the transitions with J values from 8 to 38. Our experimental line positions are in excellent agreement with those derived from molecular constants given on the literature. The observed line…

Dye laserChemistryBiophysicsAnalytical chemistryCondensed Matter PhysicsLaser linewidthsymbols.namesakeQuality (physics)TorrsymbolsCoherent anti-Stokes Raman spectroscopyFermi resonancePhysical and Theoretical ChemistryAtomic physicsRaman spectroscopyMolecular BiologyLine (formation)Molecular Physics
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Vibrational spectra and force constants of symmetric tops

1983

The infrared spectrum of H3SiI in the 800–1050 cm-1 region has been recorded with a resolution of 0·04 cm-1 and rotationally analysed. Features related to the Fermi resonance between v 5 and v 3 + v 6 and to the Coriolis x, y resonance between v 2 and v 5 have been explained, and a set of vibration-rotation parameters for the three bands has been determined by least-squares calculations, σ(J, K) = 9·4 × 10-3 cm-1. The Fermi resonance matrix element |W 356| is found to be 3·7859(7) cm-1 and the vibrational frequencies are v 2 0 = 904·551(1), v 5 0 = 941·0746(8) and (v 3 + v 6)0 = 953·688(3) cm-1. The anharmonicity constant, x 36 = -1·745(9) cm-1, has been determined. Comparison is made with …

Force constantInfraredChemistryAnharmonicityResolution (electron density)BiophysicsAnalytical chemistryResonanceCondensed Matter PhysicsMatrix elementFermi resonancePhysical and Theoretical ChemistryAtomic physicsMolecular BiologyVibrational spectraMolecular Physics
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Estimation of formamide harmonic and anharmonic modes in the Kohn-Sham limit using the polarization consistent basis sets.

2010

Formamide harmonic and anharmonic frequencies of fundamental vibrations in the gas phase and in several solvents were successfully estimated in the B3LYP Kohn-Sham complete basis set limit (KS CBS). CBS results were obtained by extrapolating a power function (two-parameter formula) to the results calculated with polarization-consistent basis sets. Anharmonic corrections using the second order perturbation treatment (PT2) and hybrid B3LYP functional combined with polarization consistent pc-n (n = 0, 1, 2, 3, 4) and several Pople’s basis sets were analyzed for all fundamental formamide vibrational modes in the gas phase and solution. Solvent effects were modeled within a PCM method. The anhar…

FormamideAcetonitrilesMolecular ConformationAnharmonic vibrationSolvent effectMolecular physicsCatalysisInorganic ChemistryAcetonechemistry.chemical_compoundComputational chemistryScissoringHexanesComputer SimulationDimethyl SulfoxideHarmonic vibrationPhysical and Theoretical ChemistryPhysics::Chemical PhysicsCarbon TetrachlorideBasis setQuantitative Biology::BiomoleculesOriginal PaperFormamidesOrganic ChemistryAnharmonicityWaterComplete basis set limitFormamideComputer Science ApplicationsComputational Theory and MathematicschemistryModels ChemicalMolecular vibrationHarmonicSolventsThermodynamicsFermi resonanceChloroformGasesSolvent effectsJournal of molecular modeling
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Raman spectroscopy of formic acid and its dimers isolated in low temperature argon matrices

2009

Raman spectroscopy combined with matrix isolation technique was employed to study formic acid monomer and its dimers. Nine fundamentals of the HCOOH monomer were identified. Additionally, the OH torsion overtone is observed and it is engaged in Fermi resonance with the δCOH mode. Several bands of the cyclic (C2h) dimer were identified and assigned. The less stable open form (Cs) of the dimer was also present in the experiment. Three intermolecular modes for the cyclic and one mode for the open dimer were found in the low frequency region. The experimental studies were supported by harmonic and anharmonic DFT calculations.

Formic acidDimerOvertoneIntermolecular forceMatrix isolationAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_compoundsymbols.namesakeMonomerchemistryPhysics::Atomic and Molecular ClusterssymbolsPhysical chemistryCondensed Matter::Strongly Correlated ElectronsFermi resonancePhysics::Chemical PhysicsPhysical and Theoretical ChemistryRaman spectroscopyChemical Physics Letters
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Photolysis of HCOOH monomer and dimer in solid argon: Raman characterization of in situ formed molecular complexes

2010

Raman spectroscopy combined with the matrix isolation technique was employed to study the 193-nm photodecomposition products of formic acid in an argon matrix. The Raman-active fundamentals belonging to the CO(2) + H(2) and CO + H(2)O photoproducts were assigned. Also, bands due to Fermi resonance between the stretching vibration (nu(1)) and the overtone of the bending mode (2nu(2)) of CO(2) were identified. Both ortho- and para-H(2) molecules were identified from their rotational lines S(0)(1) and S(0)(0), respectively. These bands appeared upon matrix annealing as well as after prolonged photolysis. Additionally, photolysis of FA dimers produces oxalic acid and its secondary photoproducts…

Formic acidStereochemistryDimerOxalic acidPhotodissociationMatrix isolationGeneral Physics and AstronomyPhotochemistrychemistry.chemical_compoundsymbols.namesakechemistryAb initio quantum chemistry methodssymbolsFermi resonancePhysical and Theoretical ChemistryRaman spectroscopyPhysical Chemistry Chemical Physics
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Characterization and Decomposition of the Natural van der Waals SnSb2Te4 under Compression

2020

[EN] High pressure X-ray diffraction, Raman scattering, and electrical measurements, together with theoretical calculations, which include the analysis of the topological electron density and electronic localization function, evidence the presence of an isostructural phase transition around 2 GPa, a Fermi resonance around 3.5 GPa, and a pressure-induced decomposition of SnSb2Te4 into the high-pressure phases of its parent binary compounds (alpha-Sb2Te3 and SnTe) above 7 GPa. The internal polyhedral compressibility, the behavior of the Raman-active modes, the electrical behavior, and the nature of its different bonds under compression have been discussed and compared with their parent binary…

Phase transitionContext (language use)[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesInorganic Chemistrysymbols.namesakeChemical structureCationsVan der Waalselectronic topologicalPhysical and Theoretical ChemistryCompressibility010405 organic chemistryChemistryCompressionDeformation0104 chemical scienceshigh pressuremetavalent bondingChemical physicsFISICA APLICADAMolecular vibration[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]symbolsCondensed Matter::Strongly Correlated ElectronsFermi resonanceSnSb2Te4pressure-induced decompositionvan der Waals forceTernary operationRaman spectroscopyRaman scatteringbonding characterInorganic Chemistry
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