CHELATION OF COPPER(II) BY DAUNOMYCIN AND 5-IMINODAUNOMYCIN AND INTERACTION OF THE COMPLEXES WITH MONONUCLEOTIDES - AN ELECTRON-SPIN-RESONANCE STUDY

Coordination of copper(II) ions by daunomycin and 5-iminodaunomycin has been studied by electron spin resonance spectroscopy, at various values of pH and r, the anthracycline-to-Cu(II) molar ratio. At r = 1-5, polymeric complexes are formed in the case of daunomycin. At r = 5, a mononuclear complex is predominant and at r = 10, this is the only one formed with the63Cu and65Cu hyperfine interaction being clearly defined in the g∥region (g∥= 2.26,63A∥= 175;65A∥= 190 G). For 5-iminodaunomycin both chelation sites are involved in the coordination and a polymeric structure (in which exchange interactions between Cu(II) centers operate) is stable in the range r = 1-3. At r = 3, the triplet state of a dinuclear Cu(II) complex is observed and 5-iminodaunomycin behaves as both a bridging and a terminal ligand. For r = 5-10, the dinuclear complex coexists with the mononuclear one. In the presence of mononucleotides dGMP, dAMP, dCMP and thymidine, no ternary complex such as mononucleotide/Cu(II)/anthracycline was observed. © 1988.