Photoisomerization of azobenzene in zeolite cavities

Cis- and trans-azobenzenes adsorbed in NaY, Na-mordenite, and Na-ZSM-5 were irradiated using 313- and 254-nm lights. The cis-trans isomer ratio in the photostationary state produced in the zeolites was compared with that in c yclohexane. It was found that Na+ in the cavities did not significantly aff ect the ratio although for stilbene a drastic change in the ratio was cause d most likely by electrostatic interaction between the carbon-carbon double bond and Na+. For azobenzene it seems probable on the basis of the results obtained by semiempirical molecular orbital calculation (AM1) that Na+ int eracts with a lone pair of one of the two nitrogen atoms, but not with the pi-orbital of the nitrogen-nitrogen double bond.