Experimental and DFT studies on the DNA-binding trend and spectral properties of complexes [Ru(bpy)2L]2+ (L = dmdpq, dpq, and dcdpq)

The trend in DNA-binding affinities and the spectral properties of a series of Ru(11) polypyridyl complexes, [Ru(bpy)(2)(dmdpq)](2+) (1), [Ru(bpy)(2)(dpq)](2+) (2), [Ru(bpy)(2)(cndpq)](2+) (3) (bpy = 2,2'-bipyridine; dpq = dipyrido[3,2-d:2',3'-f]quinoxaline; dmdpq=dimethyl-dpq; dcdpq = di-cyano-dpq), have been experimentally and theoretically investigated. The DNA-binding constants K-b of the complexes were determined systematically with spectrophotometric titration. The density functional theory (DFT) and time-dependent DFT (TDDFT) calculations were carried out for these complexes. The experimental results show that these complexes bind to DNA in intercalation mode, and the order of their intrinsic DNA-binding constants K-b is K-b(l) < K-b(2) << K-b(3). The substituents on the intercalative ligands of the complexes play a very important role in the control of DNA-binding affinities of the complexes, in particular, the stronger electron-withdrawing substituent (-CN) on the intercalative ligand can greatly improve the DNA-binding property of the derivative complex. The trend in DNA-binding affinities as well as the spectral properties of metal-ligand charge-transition ((MLCT)-M-1) of this series of complexes can be reasonably explained by applying the DFT and TDDFT calculations and the frontier molecular orbital theory. (c) 2005 Elsevier B.V. All rights reserved.