1991
DOI: 10.1021/j100164a017
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Penning ionization electron spectroscopy of dichlorobenzenes

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Cited by 18 publications
(31 citation statements)
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“…Overall, our spectrum is similar to those recorded previously using resonance line radiation [12,15,49,50] but the vibrational progressions, shown in greater detail in Figures 5, 6 and S1, are much better developed. Our discussion focusses on the photoelectron bands, due to ionisation of the 3b 1 , 2a 2 , 7b 2 or 5a 1 orbitals, where vibrational structure has been observed.…”
Section: Hei Excited Photoelectron Spectrumsupporting
confidence: 86%
“…Overall, our spectrum is similar to those recorded previously using resonance line radiation [12,15,49,50] but the vibrational progressions, shown in greater detail in Figures 5, 6 and S1, are much better developed. Our discussion focusses on the photoelectron bands, due to ionisation of the 3b 1 , 2a 2 , 7b 2 or 5a 1 orbitals, where vibrational structure has been observed.…”
Section: Hei Excited Photoelectron Spectrumsupporting
confidence: 86%
“…A closely related process was already observed for tetracyanoquinodimethane and related molecules. [44][45][46][47] In this case, however, the final product is formed without the significant rearrangement of molecular species. The high stability of these materials is substantiated by the stabilization of semiquinone radicals by high oxidation state (here d 0 ) metal centres.…”
Section: Resultsmentioning
confidence: 99%
“…For the assignment of these bands, a comparison with the spectrum of 1,3-dichlorobenzene [22,23] was helpful. Ionisations from the pyrimidine MOs π 3 , n N Ϫ and π 2 can be found in the lower energy part of the spectrum while that of n N ϩ occurs between the second and third n Cl ionisations.…”
Section: Pe Spectra and Electronic Structures Of Pyrimidines 1؊15mentioning
confidence: 99%