“…Varying the substitutive group or substituent position in the intercalative ligand can create some interesting differences in the space configuration and the electron density distribution of transition metal complexes, which will result in some differences in spectral properties and the DNA-binding behaviors of the complexes and will be helpful to more clearly understand the binding mechanism of transition metal complexes to DNA [6][7][8]. However, such studies mainly focus on the interaction of Ru(II) complexes with DNA, and the reports on the other metal complexes are relatively limited [9][10][11][12][13][14][15][16][17]. Our group has been synthesized some cobalt(III) mixedpolypyridyl complexes, which bind to DNA through an intercalative mode and promote photocleavage of plasmid pBR 322 DNA [14][15][16][17].…”