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• W4283266924 endingPage "1494" @default.
• W4283266924 startingPage "1484" @default.
• W4283266924 abstract "In the present study, the differential scattering cross-sections, depolarization ratios and Raman shifts of small molecular systems are obtained from configuration iteration wave functions of vibrational self-consistent field (VSCF) states. The transition polarizabilities were modeled using the Placzek approximation, neglecting those contributions not arising from the electric dipole mechanism. This theoretical approach is considered a good approximation for samples that absorb in the UV range if the excitation radiation falls in the visible region, as is the case of the molecules selected for the present study, namely: water, methane, and acetylene. Potential energy and electronic polarizability surfaces are calculated by the CCSD(T) and CC3 methods with aug-cc-p(C)V(T,Q,5)Z basis sets. The vibrational Hamiltonian includes the vibrational angular momentum contribution of the Watson kinetic energy operator. As expected, due to the variational nature of the VSCF and vibrational configuration interaction (VCI) methods, the Raman transition wavenumbers are substantially improved over the harmonic predictions. Surprisingly, the scattering cross-sections obtained using the harmonic approximation or the VSCF method better agrees with the experimental values than those cross-sections predicted using VCI wave functions. The more significant deviations of the VCI results from the experimental reference may be related to the significant uncertainties of the measured cross-sections. Still, it may also indicate that the VCI Raman transition moments may require a more accurate description of the electronic polarizability surface. Finally, the depolarization ratios calculated for H2 O and C2 D2 using harmonic and VCI wave functions have similar accuracy, whereas, for C2 H2 and C2 HD, the VCI results are more accurate." @default.
• W4283266924 created "2022-06-23" @default.
• W4283266924 creator A5054312591 @default.
• W4283266924 creator A5054707187 @default.
• W4283266924 date "2022-06-22" @default.
• W4283266924 modified "2023-10-16" @default.
• W4283266924 title "Calculation of absolute Raman scattering cross‐sections using vibrational self‐consistent field/vibrational configuration interaction wave functions" @default.
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• W4283266924 doi "https://doi.org/10.1002/jcc.26951" @default.
• W4283266924 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35731622" @default.
• W4283266924 hasPublicationYear "2022" @default.
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