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- W2093048175 abstract "The rotational spectra of αd1- and αd2-ortho-fluorotoluene in the ground state of the methyl group torsion have been measured. The evaluation of the spectra has been based on the theory for the internal rotation of an asymmetric internal top formulated earlier by several authors. The barrier potential being threefold symmetric (V3), each torsional level consists of three nondegenerate substates, designated as sy and ±asy. The sy-state is assigned to the conformation with the unique methyl hydrogen isotope within the molecular heavy-atom plane (sy-rotamer), while the ±asy-states belong to the respective out-of-plane conformation (asy-rotamer). In the torsional ground state the level spacing between the ±asy substates is very small and numerous accidental close degeneracies are present between the rotational level systems based on these torsional substates. The rotational levels involved are strongly perturbed by the coupling between molecular overall rotation and internal rotation. Large deviations from a rigid rotor spectrum and (+) ↔ (−) intersystem (“tunneling”) transitions are observed. The spectrum of the asy-rotamer can be well reproduced by a “two-dimensional” Hamiltonian containing 11 “rotational constants,” 9 of which are determined by a fit to the spectrum. Several are sufficiently barrier-dependent to derive V3. We obtain (in cal/mole) 567 ± 48 for αd1-ortho-fluorotoluene, 711 ± 40 for the αd2-isotope. The deviations from 649 cal/mole for the normal isotope are appreciable, probably indicating shortcomings of the semirigid model. The sy-rotamer presents a rigid rotor spectrum." @default.
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- W2093048175 date "1975-07-01" @default.
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- W2093048175 title "The microwave spectra of ortho-fluorotoluene with the asymmetric internal rotors CH2D and CD2H" @default.
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- W2093048175 doi "https://doi.org/10.1016/0022-2852(75)90042-9" @default.
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