Photofragment yield spectra of jet-cooled CH3ONO are measured over the
first few resonances of the S1 <-- S0 absorption by monitoring the NO
fragments via selected rotational levels in each of the four sublevel
s F1(A', A'') and F2 (A', A'') of the vibrational states upsilon'' = 0
, 1 and 2. Based on spectral features, the 0(0)0 transitions of the an
ti- and syn-isomers were assigned to the bands at 2 5600 +/- 30 and 26
160 +/- 30 cm-1, respectively, supporting, in combination with vibrati
onal state distributions, the dominance of a vibrationally non-adiabat
ic over an adiabatic dissociation process. The observed linewidth of t
he vibronic absorption bands of almost-equal-to 500 cm-1, which is ess
entially unchanged from that at room temperature, remains unexplained.