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Trifluoromethyl-Substituted Iridium(III) Complexes: From Photophysics to Photooxidation of a Biological Target

Photodynamic therapeutic agents are of key interest in developing new strategies to develop more specific and efficient anticancer treatments. In comparison to classical chemotherapeutic agents, the activity of photodynamic therapeutic compounds can be finely controlled thanks to the light triggerin...

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Bibliographic Details
Published in:Inorganic chemistry 2018-02, Vol.57 (3), p.1356-1367
Main Authors: Bevernaegie, Robin, Marcélis, Lionel, Laramée-Milette, Baptiste, De Winter, Julien, Robeyns, Koen, Gerbaux, Pascal, Hanan, Garry S, Elias, Benjamin
Format: Article
Language:English
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Summary:Photodynamic therapeutic agents are of key interest in developing new strategies to develop more specific and efficient anticancer treatments. In comparison to classical chemotherapeutic agents, the activity of photodynamic therapeutic compounds can be finely controlled thanks to the light triggering of their photoreactivity. The development of type I photosensitizing agents, which do not rely on the production of ROS, is highly desirable. In this context, we developed new iridium­(III) complexes which are able to photoreact with biomolecules; namely, our Ir­(III) complexes can oxidize guanine residues under visible light irradiation. We report the synthesis and extensive photophysical characterization of four new Ir­(III) complexes, [Ir­(ppyCF3)2(N^N)]+ [ppyCF3 = 2-(3,5-bis­(trifluoromethyl)­phenyl)­pyridine) and N^N = 2,2′-dipyridyl (bpy); 2-(pyridin-2-yl)­pyrazine (pzpy); 2,2′-bipyrazine (bpz); 1,4,5,8-tetraazaphenanthrene (TAP)]. In addition to an extensive experimental and theoretical study of the photophysics of these complexes, we characterize their photoreactivity toward model redox-active targets and the relevant biological target, the guanine base. We demonstrate that photoinduced electron transfer takes place between the excited Ir­(III) complex and guanine which leads to the formation of stable photoproducts, indicating that the targeted guanine is irreversibly damaged. These results pave the way to the elaboration of new type I photosensitizers for targeting cancerous cells.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.7b02778