Effect of structural change in viologen acceptors on the rate of single electron transfer from tributylphosphine

Abstract

The “flexible” 3 and “rigid” cyclic viologens 4, diquarternary salts of 2,2′-bipyridine and 1,10-phenanthroline, respectively, were treated with tributylphosphine (1) in acetonitrile containing a large amount of methanol under an argon atmosphere. A single electron transfer (SET) easily occurred from the latter to the former, the SET to 4 being 10⁵–10⁶ times faster than the SET to 3. The reorganization energy λ for the latter SET is thought to be larger than that for the former SET, because 3 undergoes a structural change upon the one-electron reduction to its radical cation, whereas the one-electron reduction of 4 takes place without a structural change. Taking into account the difference in λ, and also taking into account the bond formation energy brought about by the follow-up reaction of the phosphine radical cation 1˙⁺ with methanol, the observed kinetics were well interpreted in terms of the Marcus theory.