The photochemistry of tyrosine and tyrosine derivatives in solid polymer films (original) (raw)

The Photophysics of β-Tyrosine and Its Simple Derivatives

Journal of …, 1997

Synthesis and photophysical studies of (O-methyl)-ß-tyrosine (ß-tyrosine; an analogue of tyrosine, in which the amino group is moved from the a-to the ß-carbon, closer to the phenol ring) and its derivatives with a blocked amino and/or carboxyl group were performed to ...

Sensitized Photooxidation of Di and Tripeptides of Tyrosine

Photochemistry and Photobiology, 1998

This paper studies the dye-sensitized photooxidation of tyrosine (tyr) and tyr di- and tripeptides (tyr-tyr and tyr-tyr-tyr) mediated by singlet molecular oxygen (O,[l]) in alkaline media. Photooxidation quantum efficiencies (φr) were obtained by determining the overall and reactive rate constants of interaction with the oxidative species, employing the time-resolved O,(l) phosphorescence detection method and static-photolysis actinometric method, respectively. The interaction of O,(l)-tyr derivatives occurs through an intermediate encounter complex with polar character. Ionization of the phenolic OH group of tyr derivatives and the polarity of the solvent favors the overall interaction. Nevertheless, & values decrease when changing from water to MeCN-water medium. This indicates that the reactive deactivation of the encounter complex, probably an entropy-controlled step, may be affected by solvent polarity in the same way as those processes in which charg- es are neutralized along the reaction pathway. Photooxidation quantum efficiencies indicate that the contribution to O,(′) physical quenching (a second alternative deactivation route for the encountered complex [O,(′)-tyr derivatives]) increases with the complexity of the peptide. As a result, the selfprotection of the peptidic entity against physical quenching also increases. The information obtained from the fractional consumption mol OJmol tyr derivative (in tyr, the di- and tripeptides and the respective methyl ester of tyr and the tripeptide), together with the evolution (either consumption and/or generation) of primary amino groups upon photosensitized irradiation of the same compounds clearly indicates that the photooxidation of di- and tri-tyr peptides proceeds with the breakage of peptidic bonds. As a consequence, in the final balance each tyr unity behaves as an independent photooxidizable target.