Bimolecular self‐reactions of 2‐arylindandione‐ 1,3‐yl radicals studied by flash photolysis

Abstract

AbstractKinetic and thermodynamic data for reaction (1) of certain C‐centered aromatic radicals (referred to in this paper by the numbers I to X) in chlorobenzene: equation image have been obtained. The k1 values of radicals varied between (1.1 ± 0.2) × 106M−1·sec−1 (radical VIII) and (3.6 ± 0.7) × 109M−1 sec−1 (radical VI) at 20°C. An investigation of the relationship between the recombination rates of radicals I–VIII and X and the solvent viscosity (mixture of toluene and dibutylphthalate, 0.6 < η < 18.4 cP) has shown that the recombination reactions involving radicals I–IV are limited by diffusion in solvents having a viscosity η> 10 cP and are activation reactions in solvents having a viscosity η < 10 cP. The recombination of radicals VIII and IX is an activation reaction, while that of radicals V–VII is diffusion‐controlled in the entire viscosity range. The recombination of radical X is limited, in the viscosity range of 18.4 to 2 cP, by intrusion into the first coordination sphere of the partner, the effect of viscosity on the radical X recombination rate in the specified range being the same as its effect on diffusion‐controlled reactions. The possible reasons of the discrepancies between the experimental fast recombination rate constants and the theoretical values calculated by the Debye–Smoluchowski theory are discussed. The equilibrium constant depends strongly on the nature of the substituent in the phenyl fragment: the substituents which increase unpaired electron delocalization in the radical intensify the dissociation of the respective dimer. Long‐wave absorption bands have been recorded for radicals I–X and their extinction coefficients obtained. Dimers I–V are thermo‐ and photochromic compounds.