Kinetics and spectral characteristics of transient species formed on one-electron oxidation of acridine-1,8-dione in aqueous solution pulse radiolysis study

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Abstract
The ˙OH radicals in a neutral aqueous solution of acridine-1,8-dione (AD) have been shown to react with a bimolecular rate constant of 6.1 × 109 dm3 mol–1 s–1 and form two transient absorption bands with λmax= 320 and 650 nm. The 650 nm band is observed to decay by first-order kinetics with k= 2.2 × 103 s–1 and the 320 nm band showed mixed kinetics. Both H˙ and O˙– react with AD to form transient absorption bands with λmax= 330 and 680 nm, and are assigned to a radical species formed on H atom abstraction from a CH3 group. One-electron oxidants such as Br2˙–, N3˙– and I2˙– react with AD and form transient absorption bands with λmax= 310 and 650 nm. They are assigned to a radical species formed on deprotonation of solute radical cations at neutral pH. Based on these studies, ˙OH radicals at neutral pH are inferred to react with AD by H atom abstraction from two different sites: 38% from a CH3 group and 62% from a CH2 group which on protonation results in a solute radical cation. The 320 nm band formed on reaction of ˙OH radicals is resolved into two bands with λmax= 310 nm (radical species formed on deprotonation of solute radical cation) and 330 nm (radical formed on H atom abstraction from CH3 group). Cl2˙– is able to oxidize AD and form transient absorption bands with λmax= 305 and 560 nm which are assigned to the solute radical cation AD˙+ in acidic solutions. The pK value for the deprotonation of the solute radical cation is found to be 2.3. The I2˙–/2I– redox couple established an equilibrium with AD/AD˙+, and the oxidation potential for the AD/AD˙+ couple was determined to be 1.02 ± 0.03 V close to the half-wave potential, E1/2, value obtained electrochemically (1.17 V).

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