Ultrafast dynamics of the photochemical ring opening of 1,3-cyclohexadiene studied by multiphoton ionization

Abstract

Femtosecond time-resolved studies of the ring opening of 1,3-cyclohexadiene are presented. After absorption of a single UV photon in the region 250–270 nm (1A 1 → 1B 2 transition), the reaction is investigated using time-delayed single- and multiphoton ionization with probe pulses in the region 250–415 nm. Ions are detected by a time-of-flight mass spectrometer. The parent ion is only observed during the time when the pump and probe lasers overlap. The corresponding ionizable state, which we identify as 1B 2, has a short lifetime which we estimate to be 60 fs. The only signal detected after a delay is due to C 6H 7 +. It arises from dissociation of vibrationally hot parent ions which are produced by two-photon ionization of vibrationally excited products. The appearance rate constant of the product is as high as 1.7 ± 0.2 ps −1. It is assigned to the transition from the 2A 1 to the 1A 1 surface via a conical intersection, i.e. to the photochemical ring opening of 1,3-cyclohexadiene to Z-hexatriene. Measuring fragment ions generated by photoionization at suitable wavelengths may be a general method for monitoring vibrationally hot neutral molecules.