Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1339697 | Polyhedron | 2009 | 6 Pages |
Abstract
The phen substituted semiquinone ligand, 5,6-dioxolene-1,10-phenanthroline-O,O (sqphen), while bound to the RuII(bpy)2 moeity, oxidizes ascorbic acid and quinol at a slower rate than does the semiquinone (sq) bound to the same moiety; the basicity of sqphen decreases considerably on coordination to RuII(bpy)2, moreover, bound sqphen is less basic than bound sq, but the basicity of bound sqphen enhances on reduction to its catechol form, catphen.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Amit Mondal, Piyali De, Subrata Mukhopadhyay, Rupendranath Banerjee, Prasenjit Kar, Amilan D. Jose, Amitava Das,