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Electronic spectroscopy of jet-cooled phenylbutadienyltrimethylcyclohexene

โœ Scribed by J.P. Finley; J.R. Cable


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
518 KB
Volume
228
Category
Article
ISSN
0009-2614

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โœฆ Synopsis


The resonanceenhanced ionization spectrum of a trimethylcyclohexene compound in which the cyclohexene ring is formally conjugated to a phenylbutadienyl system has been recorded in a supersonic jet expansion. Two strong origin transitions, associated with different ground-state conformers, were identified, indicating that the electronic transition occurs with little change in torsional geometry. The frequencies at which these origin transitions occur indicate that the torsional angle between the cyclohexene double bond and the phenylbutadienyl system is 15 a from perpendicular. Similar electronic and steric forces are expected to govern the ground-state torsional geometry of the p-ionylidene ring in retinal.


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