Abstract Direct initiation of detonations in gaseous mixtures of C 2 H 2 -O 2 , H 2 -O 2 and H 2 -Cl 2 in the pressure range of 10–150 torr using flash photolysis was studied. Similar to blast initiation using a concentrated powerful energy source, it was found that for photochemical initiation, there exists a certain threshold of flash intensity and energy for each mixture at any given initial pressure and composition below which a deflagration is formed. At the critical threshold, however, a fully developed detonation is rapidly formed in the immediate vicinity of the window of incident UV radiation. However, at super critical flash energies, the amplitude of the detonation formed decreases and combustion of the entire irradiated volume approaches a constant volume explosion. It was found that photo-chemical initiation requires both a certain minimum peak value of the free radical concentration generated by the photo-dissociation as well as an appropriate gradient of this free radical distribution. The minimum peak radical concentration permits rapid reaction rates for the generation of strong pressure waves, while the gradient is necessary for the amplification of the shock waves to a detonation. If the gradient is absent and the free radicals are uniformly distributed in the mixture, then the entire volume simply explodes as in a constant volume process. The present study reveals that the mechanism of photochemical initiation is one of proper temporal synchronization of the chemical energy release to the shock wave as it propagates through the mixture. In analogy to the LASER, the term SWACER is introduced to represent this mechanism of Shock Wave Amplication by Coherent Energy Release. There are strong indications that this SWACER mechanism is universal and plays the main role in the formation of detonations whenever a powerful concentrated external source is not used to generate a strong shock wave in the explosive.