Strong-field dissociative double ionization of acetylene

We investigate dissociative double ionization of acetylene, one of the smallest organic molecules yet with a rich electronic structure, in strong laser fields by measuring two fragment ions and two electrons in coincidence. The two-body fragmentation channels are dominated by the removal of electrons from the lower-lying molecular orbitals rather than from the highest occupied one. The electron localization-assisted enhanced ionization mechanism plays a central role for the strong-field deprotonation ionization of acetylene by releasing the second electron from the up-field potential well of the hydrogen site at the internuclear distance near twice the equilibrium value of the C-H bond.