FLASH PHOTOLYSIS STUDIES ON REACTIONS BETWEEN EXCITED MOLECULES AND SELECTED SUBSTRATES. SUBSTITUENT EFFECTS IN THE CIS-TRANS ISOMERIZATION ABOUT THE CARBON-NITROGEN DOUBLE BOND.
Abstract
Ethanol solutions of N-benzylideneaniline derivatives were photoisomerized and the kinetics for the thermal relaxation was measured. This thermal reaction follows first-order kinetics and the rate constants correlate with the Hammett sigma constants. The effect of a substituent is considerably stronger when it is attached to the aniline ring than when it occupies the corresponding position on the benzaldehyde ring. This is in agreement with the non-planar model for N-benzylideneaniline, where the pi-electron system of the aniline ring interacts with the lone-pair electrons of the nitrogen atom. (Author)
Document Details
- Document Type
- Technical Report
- Publication Date
- Jan 01, 1965
- Accession Number
- AD0648440
Entities
People
- Stig Claesson
Organizations
- Uppsala University