Reactions of dichloride anion radicals with aliphatic peptides in aqueous solutions.
Author(s) -
Takahiro Masuda,
Tamon Hayashi,
Masaharu Kondo
Publication year - 1982
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.23.298
Subject(s) - chemistry , radical , reaction rate constant , flash photolysis , protonation , aqueous solution , reactivity (psychology) , photochemistry , hydrogen atom abstraction , chloride , medicinal chemistry , ion , inorganic chemistry , kinetics , organic chemistry , quantum mechanics , medicine , physics , alternative medicine , pathology
Rate constants for the reactions of dichloride anion radicals with aliphatic peptides were determined by a conventional flash photolysis of 1 M solutions of potassium chloride containing aliphatic peptides. The rate constants were found to increase with increasing number of C-H bond. Partial rate constants were assigned to each C-H bond of the aliphatic peptides, as estimated for the reactions of hydroxyl radicals with the same substrates. Trend in the partial rate constants and the effect of a protonated amino group on the reactivity indicate a reaction mechanism, hydrogen atom abstraction, similar to hydroxyl radicals.
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