IQ46can be sufficiently strong to react with the small number of the more polarizable excited molecules in solution. These, excited molecules are present in extremely small concentration, but they alone are responsible for fluorescence.We thus arrive at the conclusion that, despite apparent discrepancies, the quenching effects of purines are due to the same intermolecular forces as are responsible for their solubilizing effect and the formation of molecular compounds. SUMMARY 1. The fluorescence of polycycic aromatic hydrocarbons in aqueous caffeine solution is quenched by acidification. The quenching is reversible on neutralization. The active quenching agent is the caffeine ion, not the H-ion.2. Other purine bases, such as hypoxanthine, xanthine and N-methylxanthines, have an effect similar to that of caffeine. Uric acids quench even in pure water or aqueous ethanol, and their quenching effect is not appreciably affected by changes in the pH of the medium. A third group of purines, comprising compounds with electronegative substituents other than uric acids, and including adenine and guanine, occupy an intermediate position in that they quench without acidification, but their quenching effect is somewhat intensified in acid solution. Substances without the 4:5-double bond or the double bond adjacent to C. do not quench.3. The quenching effects are strongest in water and decrease in less polar solvents.4. The quenching is due to a reversible photochemical reaction and not to absorption of either primary or secondary radiation.5. The quenching effects were also observed with non-hydrocarbons, such as quinine sulphate, acridine sulphate, quinaldine sulphates, thiochrome, riboflavin, fluorescein. Neutral caffeine solutions sometimes exert a quenching effect, e.g. on riboflavin, and sometimes they cause an intensification of fluorescence, e.g. with thiochrome, mepacrine or eosin.6. The results are discussed, and it is concluded that, despite apparent discrepancies, the quenching effects of purines are due to the same intermolecular forces as are responsible for the solubilizing effect and the formation of molecular compounds.I am greatly indebted to Dr J. Weiss for help with the discussion part of this paper.