•  
  •  
 

Corresponding Author

Liang-nian JI

Abstract

The electrochemical characteristics and intermetallic interaction of symmetrical binurclear ruthenium (ll) complexes [Ru2 : (bpy)2Ru(DIPB)Ru(bpy)2(ClO4)4 and Ru2-2H : (bpy)2Ru(DIPB - 2H)Ru(bpy)2(ClO4)2]containing dinuclear ligand 2,2-bipyridine (bpy) andbridging ligand 1,4-di[2-imidazo[4,5-f][1,10] phenanthroine ]benzene(DIPB) or 1,4-di[2-dehydrogen-imidazo[4,5-f][1,10]phenanthroine]benzene(DIPB-2H) on a platinum electrode havebeen investigated using cyclic voltammetry, cyclic ac voltammetry and differential capacitancetechniques,etc. In acetonitrile solutions with a concentration of 0.1 mol/L TBAP, the centraruthenium ions in Ru2 and Ru2-2H complexes have shown a single 2e reversible oxidationreduction wave on the cyclic voltammograms with basically the same formal potentials of Ru2-2H andRu2 and a slightly larger apparent diffusion coefficient of the Ru2-2H complex cation than that ofRu2, i.e., 3.94 x10-6 cm2/s and 3.50 x10-6 cm2/s respectively. It appears that an enhancedelectronic interaction exists between the two central ruthenium ions in the deprotonation of thebridging ligand(DIPB).

Keywords

Binuclear ruthenium(Ⅱ) complex, Deprotonation, Electrochemical characteristics, Electronic interaction

Publication Date

2001-05-28

Online Available Date

2001-05-28

Revised Date

2000-10-30

Received Date

2000-09-29

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.