1980
DOI: 10.1088/0022-3700/13/3/023
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High resolution electron impact studies of electric dipole-forbidden states of benzene

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Cited by 33 publications
(20 citation statements)
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“…At low residual energies the spectrum is dominated by the three lowest triplet transitions in the regions 1, 2 and 3. The present low-energy (0-2 eV) forward-scattering spectra are very similar to the spectra obtained previously with intermediate (10 eV) residual energies and large scattering angles in both gaseous [4] and solid [19] phases. At 20 eV the relative intensity of the triplet states has dropped drastically and the spectrum is nearly identical to an optical absorption spectrum such as given in [ 5 ] both in relative intensities of the electronic transitions and the envelopes of the individual bands.…”
supporting
confidence: 87%
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“…At low residual energies the spectrum is dominated by the three lowest triplet transitions in the regions 1, 2 and 3. The present low-energy (0-2 eV) forward-scattering spectra are very similar to the spectra obtained previously with intermediate (10 eV) residual energies and large scattering angles in both gaseous [4] and solid [19] phases. At 20 eV the relative intensity of the triplet states has dropped drastically and the spectrum is nearly identical to an optical absorption spectrum such as given in [ 5 ] both in relative intensities of the electronic transitions and the envelopes of the individual bands.…”
supporting
confidence: 87%
“…The broad feature was not previously reported and could also correspond to the missing 'EZg transition. Detailed comparison of the present spectra with those of Wilden & Comer [4] reveal that they are consistent and the only differences stem from different relative intensities of the features under different scattering conditions. The present spectra with residual energies of 0.03 and 0.1 eV are similar to the residual energy spectrum at 60" and 10 eV of Wilden & Comer except that the improved visibility of the 3E2g state in the present study permits the location of the origin one vibrational level lower and the identification of two vibrational progressions.…”
supporting
confidence: 78%
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