Because of the nonlinearity of multiphoton ionization, an intense 5 fs puls
e is short enough to change the ionization probability from near zero to ne
ar unity in less than one-half of a laser period. For H-2(+) this exposes a
ll parts of the vibrational wave function to the full force of Coulomb repu
lsion at nearly the same time. By solving the time dependent Schrodinger eq
uation, following both electron and ion motion we show that the initial vib
rational wave function Psi(R) of H-2(+) can be reconstructed by using Coulo
mb's law to map the ion fragment kinetic energy spectrum into \Psi(R)\(2).