photometrically and spectrophotofluorometrically in several organic solvents at room temperature. A two-step photoreaction takes place, with the formation of carbazole as the main fluorescent photoproduct. In most solvents, the fluorescence intensity of diphenylamine is increased upon UV irradiation, reaching a maximum within 10 to 15 min. Photochemical-fluorescence enhancement factors range between 3 and 35. Linear log-log calibration plots are obtained over several orders of magnitude in concentration units. Photochemical-fluorimetric limits of detection are as low as 2 0 pg 1-1. The photocyclisation of diphenylamine is shown to be a very useful fluorogenic reaction for its quantitative analysis.The photocyclisation reaction of diphenylamine has been studied spectro-
INTRODUCTIONRecently, photochemical fluorogenic reactions have been proposed for improving the sensitivity and selectivity of fluorimetric detection of naturally non-fluorescent or weakly fluorescent organic compounds in bulk liquid solution (1-9) as well in combination LIith HPLC or with TLC (10-23).In the present work, we have investigated the analytical usefulness of the photocyclisation reaction of diphenylamine (Scheme I) ( 2 4 -2 8 ) for the fluorimetric determination of this compound.