Localized electron transfer and the effect of tunneling on the rates of Ru(bpy)3(2+) oxidation and reduction as measured by scanning electrochemical microscopy

Mei Shen; Allen J Bard

doi:10.1021/ja206136h

Localized electron transfer and the effect of tunneling on the rates of Ru(bpy)3(2+) oxidation and reduction as measured by scanning electrochemical microscopy

J Am Chem Soc. 2011 Oct 5;133(39):15737-42. doi: 10.1021/ja206136h. Epub 2011 Sep 8.

Authors

Mei Shen¹, Allen J Bard

Affiliation

¹ Center for Electrochemistry, Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station, A5300, Austin, Texas 78712-0165, United States.

PMID: 21842886
DOI: 10.1021/ja206136h

Abstract

The kinetics of tris(2,2'-bipyridine)ruthenium(II) (Ru(bpy)) oxidation and reduction in acetonitrile were investigated by steady-state voltammetry using scanning electrochemical microscopy (SECM). The SECM setup was placed inside a drybox for carrying out experiments in an anhydrous atmosphere and in the absence of oxygen. The standard rate constant, k°, for Ru(bpy) oxidation at a Pt electrode (radius, a = 5 μm) was 0.7 ± 0.1 cm/s, which is smaller than k° for Ru(bpy) reduction measured under the same conditions (≥3 cm/s). This is attributed to the 2,2'-bipyridine ligands having an electron-transfer (ET) blocking effect on the oxidation of the ruthenium(II) center, as opposed to the reduction, which involves ET to the exposed ligands. Thus, tunneling effects may be important in considering the ET in this molecule.