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Hydrogen evolution from the photolysis of alcoholic benzophenone solutions via redox catalysis

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00520a032· OSTI ID:5666754
The overall process catalyzed by the platinum sol is the benzophenone-sensitized dehydrogenation of 2-propanol. The standard enthalpy of the reaction is positive, which makes this process light energy storing. The mechanism derived from the laser photolysis studies is corroborated by results obtained from continuous illumination of alcoholic benzophenone solution. Spectrophotometric data obtained before and after irradiation of samples with and without catalyst are compared. In the case of the Pt-free solution a photolysis time of 30 m suffices to remove >70% of the benzophenone absorption at 260 nm. In contrast, one finds practically no depletion of benzophenone under illumination if the platinum catalyst is present. Hydrogen is evolved, as shown by gas chromatographic analysis. The catalyst can intervene efficiently to prevent ketyl radical dismutation making feasible stoichiometric water reduction. In the presence of Pt catalyst, benzophenone sensitizes the dehydrogenation of 2-propanol to acetone. 2 figures.
Research Organization:
Ecole Polytechnique Federale, Lausanne, Switzerland
OSTI ID:
5666754
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 101:26; ISSN JACSA
Country of Publication:
United States
Language:
English

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