Tris-ruthenium(II)/copper(II) multimetallic porphyrin: Synthesis, characterization, DNA binding and supercoiled DNA photocleavage studies |
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Authors: | Emily Craver Mark Nielsen |
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Affiliation: | a Department of Biology, University of Dayton, 300 College Park, Dayton, OH 45469-2320, United States b Department of Chemistry, University of Dayton, 300 College Park, Dayton, OH 45469-2357, United States |
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Abstract: | The porphyrin, meso-5-(pentafluorophenyl)-10, 15, 20-tris(4-pyridyl)porphyrin has been used to synthesize two new metalloporphyrin complexes. Insertion of copper(II) into the porphyrin center gives the copper(II) porphyrin. Coordination of three [Ru(bipy)2Cl]+ moieties (where bipy = 2,2′-bipyridine) to the pyridyl nitrogens of the copper(II) porphyrin gives the target complex. Electronic transitions associated with the copper(II) porphyrin and the triruthenium copper(II) porphyrin include an intense Soret band and a less intense Q-band in the visible region of the spectrum. An intense π-π∗ transition in the UV region associated with the bipyridyl groups and a metal to ligand charge transfer (MLCT) band appearing as a shoulder to the Soret band are observed for the ruthenated copper(II) porphyrin. Electrochemical properties associated with the multimetallic complex include a redox couple in the cathodic region with E1/2 = −0.86 V versus Ag/AgCl attributed to the porphyrin and a redox couple in the anodic region E1/2 = 0.88 V versus Ag/AgCl due to the RuIII/II couple. DNA titrations indicate the triruthenium copper(II) porphyrin interacts with DNA potentially through a groove binding mechanism. Irradiation of aqueous solutions of the target complex and supercoiled DNA at a 10:1 base pair to complex ratio with visible light above 400 nm indicates that the complex causes nicking of the DNA helix. |
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Keywords: | Photodynamic therapy Copper porphyrin Ruthenium DNA binding DNA photocleavage |
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