We examine the possibility that three hydrogen atoms
in one plane
of the cyclopropane dication come together in a concerted “ring-closing”
mechanism to form H3
+, a crucial cation in interstellar gas-phase chemistry. Ultrafast
strong-field ionization followed by disruptive probing measurements
indicates that the formation time of H3
+ is 249 ± 16 fs. This time scale
is not consistent with a concerted mechanism, but rather a process
that is preceded by ring opening. Measurements on propene, an isomer
of cyclopropane, reveal the H3
+ formation time to be 225 ± 13 fs, a time
scale similar to the H3
+ formation time in cyclopropane. Ab initio molecular dynamics
simulations and the fact that both dications share a common potential
energy surface support the ring-opening mechanism. The reaction mechanism
following double ionization of cyclopropane involves ring opening,
then H-migration, and roaming of a neutral H2 molecule,
which then abstracts a proton to form H3
+. These
results further our understanding of complex interstellar chemical
reactions and gas-phase reaction dynamics relevant to electron ionization
mass spectrometry.