Laser-induced fluorescence from the CH3I-Cl and ICH2I-Cl adducts formed in association reactions between chlorine atoms and CH3I and CH2I2 has been observed for the first time. The LIF excitation and dispersed fluorescence spectra have been measured in the range 345-375 nm and 380-480 nm, respectively, at 204 and 296 K. The excitation spectra exhibit vibrational fine structure, and a semiquantitative analysis of the spectra yields a similar binding energy for both adducts of similar to 60 kJ mol(-1). The adduct fluorescence is efficiently quenched by N-2 and exhibits a zero-pressure lifetime of similar to 25 - 30 ns. Using LIF excited from the CH3I-Cl and ICH2I-Cl adducts, the kinetics of the reactions of atomic chlorine with methyl iodide and diiodomethane have been investigated, the results showing that both reactions proceed via two independent channels, an association reaction to form the adduct and a bimolecular abstraction reaction. At T - 200 K, the association reaction is predominant, and CH3I-Cl formation is irreversible, with rate coefficients for adduct formation found to be pressure-dependent and in reasonable agreement with the literature. At similar to 200 K, removal of the adduct is dominated by reaction with radical species (CH3 and CISO) and by self-reaction, which proceed at close to the gas kinetic limit. At 296 K, CH3I-Cl formation is reversible, and the equilibrium constant, K-p = (70.9 +/- 27.4) x 10(3) atm(-1), was determined, which is in excellent agreement with the literature, and the adduct does not significantly react with CH3I. The uncertainty is at the 95% confidence level (2 sigma) and includes systematic errors. At similar to 200 K, the ICH2I-Cl adduct is again stabilized, with pressure-dependent rate coefficients reaching the high pressure limit at lower pressures than for the Cl + CH3I reaction. At room temperature, the ICH2I-Cl adduct is removed via an additional unimolecular decomposition channel, which dominates over the reversible decomposition channel to reform Cl + CH,,I,. Neither adduct was observed to undergo significant reaction with molecular oxygen at similar to 200 or 296 K, with an upper limit rate coefficient determined as k < 10(-16) cm(3) molecule(-1) s(-1).