G. Epling, Wells Jn, U. Yoon
Feb 1, 1988
Citations
0
Influential Citations
9
Citations
Journal
Photochemistry and Photobiology
Abstract
Abstract— The photochemical transformations of 3,3′,4′,5‐tetrachlorosalicylanilide, have been characterized by isolation and spectroscopic determination of the primary and secondary photoproducts. The photoreactivity cleanly involves photochemical dechlorination; three chlorines are ultimately lost in an efficient stepwise fashion. A radical mechanism was implicated by formation of a dimer and hydrogen atom abstraction from cysteine when present during photolysis. In the presence of HSA or BSA, the initial dehalogenation leads to a photoadduct with the protein, but dehalogenation of the primary photoproduct, a trichloro compound, does not lead to an efficient photobinding to protein.