Photolysis of formylmethylflavin in aqueous and organic solvents

• Published in: Photochemical & photobiological sciences 2006-07, Vol.5 (7), p.680-685
• Main Authors: Ahmad, Iqbal, Fasihullah, Q, Vaid, Faiyaz H M
• Format: Article
• Language: English
• Subjects: Flavins - chemistry; Kinetics; Molecular Structure; Photolysis; Riboflavin - chemistry; Solvents - chemistry; Time Factors
• ISSN: 1474-905X; 1474-9092
• DOI: 10.1039/b602917e

The photolysis of formylmethylflavin (FMF), a major intermediate in the photodegradation sequence of riboflavin, has been carried out in water (pH 7.0) and in several organic solvents. FMF produces lumichrome (LC) in organic solvents and LC and lumiflavin (LF) in aqueous solution. FMF and its photoproducts have been analysed using a specific multicomponent spectrophotometric method. FMF undergoes a bimolecular redox reaction on photolysis. The second-order rate constants for the reaction range from 0.66 (chloroform) to 2.44 M(-1) s(-1) (water) and are a linear function of the solvent dielectric constant. A plot of ln k against 1/epsilon is linear for the reactions in 1-butanol, 1-propanol, ethanol, methanol, acetonitrile and water (epsilon approximately 17-79) and non-linear in chloroform and dichloroethane (epsilon approximately 5-10) suggesting a change in reaction mechanism in the two regions. This may be explained on the basis of the existence of a dipolar intermediate along the reaction pathway. The rate of photolysis is governed by the solvation of the intermediate and is thus influenced by the dielectric constant of the medium. The solvent effect on the rate of photolysis of FMF has been expressed in terms of the solvent acceptor number. A linear relationship has been found between ln k and the solvent acceptor number.