Fermi-phase-induced interference in the reaction between Cl and vibrationally excited CH 3 D.

Mode selectivity is a well-established concept in chemical dynamics. A polyatomic molecule possesses multiple vibrational modes and the mechanical couplings between them can result in complicated anharmonic motions that defy a simple oscillatory description. A prototypical example of this is Fermi-coupled vibration, in which an energy-split eigenstate executes coherent nuclear motion that is comprised of the constituent normal modes with distinctive phases. Will this vibrational phase affect chemical reactivity? How can this phase effect be disentangled from more classical amplitude effects? Here, to address these questions, we study the reaction of Cl with a pair of Fermi states of CH 3 D(v 1 -I and v 1 -II). We find that the reactivity ratio of (v 1 -I)/(v 1 -II) in forming the CH 2 D(v = 0) + HCl(v) products deviates significantly from that permitted by the conventional reactivity-borrowing framework. Based on a proposed metric, this discrepancy can only be explained when the scattering interferences mediated by the CH 3 D vibrational phases are explicitly considered, which expands the concept of vibrational control of chemical reactivity into the quantum regime.