A definitive example of a geometric "entatic state" effect: Electron-transfer kinetics for a copper(ll/l) complex involving a quinquedentate macrocyclic trithiaether - Bipyridine ligand

The quinquedentate macrocyclic ligand cyclo-6,6′-[1,9-(2,5,8- trithianonane)]-2,2′-bipyridine ([15]aneS₃bpy = L), containing two pyridyl nitrogens and three thiaether sulfurs as donor atoms, has been synthesized and complexed with copper. The Cu^II/I redox potential, the stabilities of the oxidized and reduced complex, and the oxidation and reduction electron-transfer kinetics of the complex reacting with a series of six counter reagents have been studied in acetonitrile at 25°C, μ = 0.10 M (NaCIO₄). The Marcus cross relationship has been applied to the rate constants obtained for the reactions with each of the six counter reagents to permit the evaluation of the electron self-exchange rate constant, k ₁₁. The latter value has also been determined independently from NMR line-broadening experiments. The cumulative data are consistent with a value of k₁₁ = 1 × 10⁵ M^-1 s¹, ranking this among the fastest-reacting Cu^II/I systems, on a par with the blue copper proteins known as cupredoxins. The resolved crystal structures show that the geometry of the Cu^IIL and Cu^IL complexes are nearly identical, both exhibiting a five-coordinate square pyramidal geometry with the central sulfur donor atom occupying the apical site. The most notable geometric difference is a puckering of an ethylene bridge between two sulfur donor atoms in the Cu^IL complex. Theoretical calculations suggest that the reorganizational energy is relatively small, with the transition-state geometry more closely approximating the geometry of the Cu^IIL ground state. The combination of a nearly constant geometry and a large self-exchange rate constant implies that this Cu^II/I redox system represents a true geometric "entatic state."