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- W2024886462 abstract "Abstract An alternative procedure for the calculation of highly excited vibrational levels in S0 formaldehyde was developed to apply to larger molecules. It is based on a new set of symmetrized vibrational valence coordinates. The fully symmetrized vibrational kinetic energy operator is derived in these coordinates using the Handy expression [Molec. Phys. 61, 207 (1987)]. The potential energy surface is expressed as a fully symmetrized quartic expansion in the coordinates. We have performed ab initio electronic computations using GAMESS to obtain all force constants of the S0 formaldehyde quartic force field. Our large scale vibrational calculations are based on a fully symmetrized vibrational basis set, in product form. The vibrational levels are calculated one by one using an artificial intelligence search/selection procedure and subsequent Lanczos iteration, providing access to extremely high vibrational energies. In this work special attention has been given to the CH stretch system by calculating the energies up to the fifth CH stretch overtone at ∼16000 cm−1, but the method has also been tested on two highly excited combination levels including other lower frequency modes." @default.
- W2024886462 created "2016-06-24" @default.
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- W2024886462 date "2011-06-04" @default.
- W2024886462 modified "2023-09-27" @default.
- W2024886462 title "Vibrational calculations in formaldehyde: the CH stretch system" @default.
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- W2024886462 doi "https://doi.org/10.2478/s11532-011-0042-6" @default.
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