Four azobenzene amphiphiles containing tertiary amide groups were synt
hesized and characterized. Reversible cis/trans photoisomerization of
these compounds has been studied in solutions by irradiation with UV l
ight at 335 nm and visible light at 452 nm. Stability of the monomolec
ular layer, the collapse pressure, and the molecular area have been in
vestigated as a function of chemical structure of azobenzene derivativ
e and of equilibrium concentration of the cis and trans form in spread
ing solution.