Thermal and photochemical reduction of aqueous chlorine by ruthenium(II) polypyridyl complexes.

Abstract

Studies are reported on the reactions of aqueous chlorine with a series of substitution-inert, one-electron metal-complex reductants, which includes [Ru(bpy)3]2+, [Ru(4,4'-Me2bpy)3]2+, [Ru(4,7-Me2phen)3]2+, [Ru(terpy)2]2+, and [Fe(3,4,7,8-Me4phen)3]2+. The reactions were studied by spectrophotometry at 25 degrees C in acidic chloride media at mu = 0.3 M. In general the reactions have the stoichiometry 2[ML3]2+ + Cl2-->2[ML3]3+ + 2Cl-. In the case of [Ru(bpy)3]2+, the reaction is quite photosensitive; the thermal reaction is so slow as to be practically immeasurable. The reactions of [Ru(4,4'-Me2bpy)3]2+ and [Ru(4,7-Me2phen)3]2+ are also highly photosensitive, giving pseudo-first-order rate constants that depend on the monochromator slit width in a stopped-flow instrument; however, the thermal rates are fast enough that they can be obtained by extrapolation of kobs to zero slit width. The reactions of [Ru(terpy)2]2+ and [Fe(3,4,7,8-Me4phen)3]2+ show no appreciable photosensitivity, allowing direct determination of their thermal rate laws. From the kinetic effects of pH, [Cl2]tot, and [Cl-] it is evident that all of the thermal rate laws have a first-order dependence on [ML3]2+ and on [Cl2]. The second-order rate constants decrease as Eo for the complex increases, consistent with the predictions of Marcus theory for an outer-sphere electron-transfer mechanism. Quantum yields at 460 nm for the reactions of [Ru(4,4'-Me2bpy)3]2+ and [Ru(4,7-Me2phen)3]2+ exceed 0.1 and show a dependence on [Cl2] indicative of competition among spontaneous decay of *Ru, nonreactive quenching by Cl2, and reactive quenching by Cl2.