Emission spectra following the photolysis of iodomethanes (CHI3, CH2I2, CH3I, and CH2ICl) at 266 nm were recorded in a slow flow cell. In addition to emission from the electronically excited species including CH (A(2)Δ, B(2)Σ(-), and C(2)Σ(+)), C2 (d(3)Πg), and atomic iodine ((4)P(o)), a series of emission bands was observed in the 12,000-19,000 cm(-1) region. The dominant structure of these emission bands was verified as the I2 B(3)Π(+)(0,u)-X(1)Σ(+)g emission at the 532 nm excitation, and the observed I2 was formed from collisions between iodine atoms generated from the C-I bond dissociation in these iodomethanes. The I2 emission spectra following the photolysis of CH2I2 at different wavelengths were acquired, and the threshold energy for the first C-I bond cleavage was determined to be 208 ± 1 kJ mol(-1). We also obtained the emission spectra of pure I2 at several visible excitation wavelengths for comparison with those from the photolysis of iodomethanes, and a least-squares global fit of the observed I2 emission bands yields more accurate anharmonicity parameters for the vibrational structure in the I2 B-X transition.