We obtained state-specific photofragment yield (PHOFRY) spectra of jet
-cooled CH3ONO in the S1 <-- S0 absorption system by monitoring select
ed rotational levels in NO v = 0, 1 and 2. The spectra exhibit bands w
hich are assigned to both the syn- and anti-rotamers with origins at 3
80 nm and 388 nm, respectively. All the bands are broad (500-800 cm-1)
suggesting that the dissociation lifetimes are shorter than those obt
ained in dynamical calculations on model potential energy surfaces. Th
e widths do not depend on the monitored NO rotational level. The resul
ts support a mechanism where nonadiabatic vibrational predissociation
is preferred.