Jahn-Teller effects in molecular cations studied by photoelectron spectroscopy and group theory.

The traditional "ball-and-stick" concept of molecular structure fails when the motion of the electrons is coupled to that of the nuclei. Such a situation arises in the Jahn-Teller (JT) effect which is very common in open-shell molecular systems, such as radicals or ions. The JT effect is well known to chemists as a mechanism that causes the distortion of an otherwise symmetric system. Its implications on the dynamics of molecules still represent unsolved problems in many cases. Herein we review recent progress in understanding the dynamic structure of molecular cations that have a high permutational symmetry by using rotationally resolved photoelectron spectroscopy and group theory. Specifically, we show how the pseudo-Jahn-Teller effect in the cyclopentadienyl cation causes electronic localization and nuclear delocalization. The fundamental physical mechanisms underlying the vaguely defined concept of "antiaromaticity" are thereby elucidated. Our investigation of the methane cation represents the first experimental characterization of the JT effect in a threefold degenerate electronic state. A special kind of isomerism resulting from the JT effect has been discovered and is predicted to exist in all JT systems in which the minima on the potential-energy surface are separated by substantial barriers.