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Tridiagonal Fermi resonance structure in the vibrational spectrum of the CH chromophore in CHF3. II. Visible spectra
148
Citations
43
References
1987
Year
EngineeringOvertone Band StrengthsChemistryNear IrSpectroscopic PropertySpectra-structure CorrelationNuclear Quadrupole ResonanceIntense Cf3Molecular SpectroscopyPhysicsAtomic PhysicsCh ChromophorePhysical ChemistryQuantum ChemistryVisible SpectraSpectroscopyNatural SciencesResonanceVibrational Spectrum
The near IR and visible vibrational absorption spectra of CHF3 were recorded up to wave numbers of 17 500 cm−1 providing complete frequency coverage, together with paper I, from the low frequency fundamentals to the N=6 CH stretching–bending overtone multiplet. All strong bands in the high overtone spectra could be predicted and assigned by means of the tridiagonal Fermi resonance Hamiltonian, including a few combinations with intense CF3 stretching vibrations already observed for the low overtones. Improved vibrational Fermi resonance constants are presented on the basis of a fit to 35 assigned bands. An analysis of the rotational fine structure of the 2ν4 (E) overtone component and several Fermi resonance component bands result in values for αb and αs, which allow us to determine Be. In the high overtone bands no rotational fine structure is observed. The bands can be understood by introducing additional homogeneous rovibrational structures of phenomenological widths Γ≊1 to 10 cm−1. The results are discussed in relation to the separation of time scales for mode selective vibrational redistribution and further evolution. The overtone band strengths are reported and analyzed approximately with the empirical local Mecke dipole function.
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