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• W2023015058 endingPage "3602" @default.
• W2023015058 startingPage "3588" @default.
• W2023015058 abstract "The pure rotational spectrum in the far-infrared and its absolute intensity in the vibrational ground state of CHD3 and CH3D, and the integrated band strength of the N=5 CH-stretching overtone of CHD3 in the near infrared to visible were measured by high-resolution interferometric Fourier transform techniques. The far-infrared data result in permanent electric dipole moments (‖μz0‖=(5.69±0.14)×10−3 D for CHD3, ‖μz0‖=(5.57±0.10)×10−3 D for CH3D), consistent with previous experimental data. The integrated N=5 overtone cross section is found to be (0.828±0.068) fm2. The overtone data are used, together with previous data, to derive a new, nine-dimensional, isotopically invariant dipole moment function for CH4 within the chromophore model for the CH chromophore in CHD3. With this function, the experimental data can be reproduced to an averaged factor of 1.2, in the best case. In the vibrational ground state, a nine-dimensional calculation of expectation values on a new, fully anharmonic potential surface was performed using the solution of the rovibrational Schrödinger equation by diffusion quantum Monte Carlo methods. The results for the rotational constants of several isotopomers, which include significant contributions from rovibrational interactions, indicate that the equilibrium CH bond length of methane is re=108.6 pm. The calculated value for the vibrationally averaged permanent dipole moment from these nine-dimensional vibrational quantum calculations, using the dipole moment function consistent with the analysis of the overtone bands, is μz0=−(6.6±0.4)×10−3 D for CHD3 (with positive z coordinate for the H atom) and μz0=(6.8±0.5)×10−3 D for CH3D (with positive z coordinate for the D atom) in essential agreement with the far-infrared rotational intensities. The sign could be determined unambiguously by comparison with ab initio data. We predict the permanent dipole moment of several further methane isotopomers. The polarity of the CH bond in methane is C−–H+, within our simple bond dipole model, but is discussed to be a model dependent (not purely experimental) quantity." @default.
• W2023015058 created "2016-06-24" @default.
• W2023015058 creator A5019428571 @default.
• W2023015058 creator A5026742233 @default.
• W2023015058 creator A5043072345 @default.
• W2023015058 creator A5057119611 @default.
• W2023015058 date "1994-09-01" @default.
• W2023015058 modified "2023-10-16" @default.
• W2023015058 title "Dipole moment function and equilibrium structure of methane in an analytical, anharmonic nine-dimensional potential surface related to experimental rotational constants and transition moments by quantum Monte Carlo calculations" @default.
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• W2023015058 doi "https://doi.org/10.1063/1.467544" @default.
• W2023015058 hasPublicationYear "1994" @default.
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