A Definitive Example of a Geometric “Entatic State” Effect:
Electron-Transfer Kinetics for a Copper(II/I) Complex Involving
A Quinquedentate Macrocyclic Trithiaether−Bipyridine Ligand
ChakaGezahegn
SonnenbergJason L.
SchlegelH. Bernhard
HeegMary Jane
JaegerGregory
NelsonTimothy J.
OchrymowyczL. A.
RorabacherD. B.
2007
The quinquedentate macrocyclic ligand cyclo-6,6‘-[1,9-(2,5,8-trithianonane)]-2,2‘-bipyridine
([15]aneS<sub>3</sub>bpy = L), containing two pyridyl nitrogens and three thiaether sulfurs as donor atoms, has been
synthesized and complexed with copper. The Cu<sup>II/I</sup>L 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 (NaClO<sub>4</sub>). 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, <i>k</i><sub>11</sub>. The
latter value has also been determined independently from NMR line-broadening experiments. The cumulative
data are consistent with a value of <i>k</i><sub>11</sub> = 1 × 10<sup>5</sup> M<sup>-1</sup> s<sup>-1</sup>, ranking this among the fastest-reacting Cu<sup>II/I</sup>
systems, on a par with the blue copper proteins known as cupredoxins. The resolved crystal structures
show that the geometry of the Cu<sup>II</sup>L and Cu<sup>I</sup>L 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<sup>I</sup>L
complex. Theoretical calculations suggest that the reorganizational energy is relatively small, with the
transition-state geometry more closely approximating the geometry of the Cu<sup>II</sup>L ground state. The
combination of a nearly constant geometry and a large self-exchange rate constant implies that this Cu<sup>II/I</sup>
redox system represents a true geometric “entatic state.”