Abstract:Abstract-5,8-dihydroxy-1,4-dihydro-1,4-methanonaphthalene (DDMN), a substituted phenol, is synthesized by reduction of a cyclic dione, 1,4,4a,8a-tetrahydro-endo-1,4-methano-naphtha-5,8-dione (THMND). Pulse radiolysis technique has been employed to understand the nature of transient species formed on reaction of radiolytic species of water radiolysis with DDMN.• OH radicals were observed to react with DDMN with a bimolecular rate constant of 1.5 × 10 10 dm 3 mol −1 s −1 . Inhibition of radiation induced lipid-p… Show more
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