Journal of Physical Chemistry p. 1788 - 1795 (1983)
Update date:2022-08-10
Topics:
Kelsall, Benuel J.
Andrews, Lester
McGarvey, Glenn J.
Matrix photoionization experiments have been performed for several p-dialkylbenzenes and alkylcycloheptatrienes.Broad absorptions at 23500 and 34700 cm-1 following UV matrix two-photon ionization of p-xylene are assigned to the parent cation, in agreement with photodissociation spectra of gaseous cation.A broad absorption at 20240 cm-1 following vacuum-UV matrix photoionization of 7-methylcycloheptatriene is assigned to the parent cation, in agreement with the difference between photoelectron bands.Mercury arc photolysis has been used to activate the extensive rearrangements of the p-xylene and 7-methylcycloheptatriene cations, which finally rearrange to a common conjugated triene cation identified as a substituted methylenecyclohexadiene cation.
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