Ultrafast Ring Closure Reaction of Gaseous <i>cis</i>-Stilbene from S<sub>1</sub>(ππ*)
Shutaro Karashima, Xincheng Miao, Akio Kanayama, Yoichi Yamamoto, Junichi Nishitani, Nikita Kavka, Roland Mitrić, Toshinori Suzuki
Abstract
cis -Stilbene ( cis -St) is a well-known benchmark system for cis – trans photoisomerization. cis -St also produces 4a,4b-dihydrophenanthrene (DHP) in solution with a quantum yield of less than 0.19. The ring closure reaction, however, has never been identified for gaseous cis -St, and a recent computational simulation predicted the quantum yield of DHP to be only 0.04. In the present study, we identified an ultrafast ring closure reaction of gaseous cis -St for the first time using extreme ultraviolet time-resolved photoelectron spectroscopy. Surface hopping trajectory calculations at the SA3-XMS-CASPT2(2,2) level of theory reproduce the features of the observed time-resolved photoelectron spectra and predict the cis -St:DHP: trans -St branching ratio to be 0.55:0.41:0.04, in contrast with previous estimates. The results indicate that photoexcited cis -St favors ring closure over cis – trans isomerization under the isolated condition.