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Photooxidation of Methionine Derivatives by the 4‐Carboxybenzophenone Triplet State in Aqueous Solution. Intracomplex Proton Transfer Involving the Amino Group
Author(s) -
Hug Gordon L.,
Bobrowski Krzysztof,
Kozubek Halina,
Marciniak Bronislaw
Publication year - 1998
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1998.tb05285.x
Subject(s) - chemistry , deprotonation , flash photolysis , photochemistry , cationic polymerization , electron transfer , aqueous solution , radical ion , reaction rate constant , quenching (fluorescence) , sulfur , ion , fluorescence , organic chemistry , kinetics , physics , quantum mechanics
— Oxidation of the triplet state of 4‐carboxybenzophenone (CB) by a series of five substituted methionines and three methionine‐containing dipeptides was monitored under laser flash photolysis conditions in aqueous solution. Spectral resolution techniques were employed to follow the concentration profiles of the intermediates formed from the quenching events. From these concentration profiles, quantum yields for the intermediates were determined. Branching ratios were evaluated for the decay of the charge‐transfer complex by the competing processes of back electron transfer, proton transfer and escape of radical ions. The relative prominence of these processes was discussed in terms of the proton‐transfer tendencies of the nominal sulfur‐radical‐cationic species. A systematic decrease was observed in the quantum yields for the escape of radical ions along with a correlated increase in the proton‐transfer yields. The enhanced propensity of the sulfur radical cations to depro‐tonate is due to deprotonation at the carbons adjacent to the sulfur‐cationic site and at the unsubstituted amino groups when present. This scheme was supported by an observed decrease in the yields of dimeric sulfur radical cations with an increase in the electron‐withdrawing abilities of the substituents, making the radical‐cationic species stronger acids. The involvement of protons on the amino groups was implicated by the correlation of the quantum yields of ketyl radical formation in the photochemistry experiments with the rate constants for the reaction of the CB radical anion with the sulfur‐containing substrates in pulse radiolysis experiments.