Revealing electronic state-switching at conical intersections in alkyl iodides by ultrafast XUV transient absorption spectroscopy.

Abstract

Conical intersections between electronic states often dictate the chemistry of photoexcited molecules. Recently developed sources of ultrashort extreme ultraviolet (XUV) pulses tuned to element-specific transitions in molecules allow for the unambiguous detection of electronic state-switching at a conical intersection. Here, the fragmentation of photoexcited iso-propyl iodide and tert-butyl iodide molecules (i-C₃H₇I and t-C₄H₉I) through a conical intersection between ³Q₀/¹Q₁ spin-orbit states is revealed by ultrafast XUV transient absorption measuring iodine 4d core-to-valence transitions. The electronic state-sensitivity of the technique allows for a complete mapping of molecular dissociation from photoexcitation to photoproducts. In both molecules, the sub-100 fs transfer of a photoexcited wave packet from the ³Q₀ state into the ¹Q₁ state at the conical intersection is captured. The results show how differences in the electronic state-switching of the wave packet in i-C₃H₇I and t-C₄H₉I directly lead to differences in the photoproduct branching ratio of the two systems.