The catalytic activity of dioxo-molybdenum(VI)-dichloro[4,4 0 -dicarboxylato-2,2 0 -bipyridine] covalently anchored through the carboxylate function to the surface of TiO 2 has been tested for the oxidative degradation of 1-chloro-4-ethylbenzene in MeCN solution under argon and UV irradiation (k = 254 nm). After 4-5 h of photochemical reaction, the Mo complex was reoxidized in the presence of O 2 in the dark, and then the reaction was continued under argon. The reaction proceeds by the intermediate formation of 4 0 -chloroacetophenone that undergoes further decomposition to chlorobenzene, plus small amounts of oxygen-containing organochlorine compounds, CO 2 and H 2 O. Similar results were obtained for the decomposition of 4 0 -chloroacetophenone under the same conditions, which also gave chlorobenzene as one of the main products. The ratio of [final product]/ [Mo complex] increases during the decomposition of 1-chloro-4-ethylbenzene (up to 350-400% for 30-35 h of reaction), which provides evidence of a catalytic process. The probable photochemical reactions are discussed.