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Updated: Jun 14, 2026

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Unusual photophysical properties of a ruthenium(II) complex related to [Ru(bpy)2(dppz)]2+
Yujie Sun1, Sibrina N Collins, Lauren E Joyce
1Department of Chemistry, The Ohio State University, Columbus, Ohio 43210, USA.
Abstract:
A new ruthenium polypyridyl complex, [Ru(bpy)(2)(dpqp)](2+) (bpy = 2,2'-bipyridne; dpqp = pyrazino[2',3':5,6]pyrazino[2,3-f][1,10]phenanthroline), shows strong luminescence in water at room temperature, a behavior that is strikingly different from that of the nonemissive "DNA light-switch" prototype [Ru(bpy)(2)(dppz)](2+) (dppz = dipyrido[3,2-a:2'-3'-c]phenazine) under similar conditions. Variation of the absorption and emission spectra of [Ru(bpy)(2)(dpqp)](2+) as a function of the pH is consistent with the occurrence of two ground-state protonation steps associated with the dpqp ligand and an apparent pK(a)* of 2.1. Electrochemistry and theoretical calculations indicate that the lowest unoccupied molecular orbital (LUMO) of [Ru(bpy)(2)(dpqp)](2+) is localized on the distal portion of the dpqp ligand and lies at a lower energy than the dppz-based LUMO of [Ru(bpy)(2)(dppz)](2+). The combination of its strong DNA binding affinity and relatively long-lived triplet metal-to-ligand charge-transfer excited state in an aqueous solution results in more efficient DNA photocleavage by [Ru(bpy)(2)(dpqp)](2+) than [Ru(bpy)(2)(dppz)](2+).
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