Iridium(iii) polypyridine complexes with a disulfide linker as biological sensors and cytotoxic agents.

The synthesis, characterization, and photophysical properties of two novel cyclometalated iridium(iii) PEG complexes with a disulfide linkage Ir(N^C)2(bpy-SS-PEG) (bpy-SS-PEG = 4-(N-(2-((N-(2-(ω-methoxypoly(1-oxapropyl))ethyl)amino)cabonylethoxy)dithiolethoxy)carbonylamino)methyl-4'-methyl-2,2'-bipyridine; HN^C = methyl 2-phenyl-4-quinolinecarboxylate (pqe) (1a), 2-phenylquinoline (pq) (2a)), their PEG-free counterparts Ir(N^C)2(bpy-SS-py) (HN^C = pqe (1b), pq (2b)), their disulfide-free counterparts Ir(N^C)2(bpy-CONH-PEG) (bpy-CONH-PEG = 4-N-(2-(ω-methoxypoly-(1-oxapropyl))ethyl)aminocarbonyl)-4'-methyl-2,2'-bipyridine; (HN^C = pqe (1c), pq (2c)), and a bimetallic iridium(iii)-rhenium(i) complex Ir(pqe)2(bpy-SS-py)Re(Me4-phen)(CO)3(CF3SO3) (Me4-phen = 3,4,7,8-tetramethyl-1,10-phenathroline) (3) are reported. Upon irradiation, the complexes displayed intense green to red emission under ambient conditions. Complex 3 containing two communicating luminophores exhibited large spectral overlap and was found to have a theoretical FRET efficiency of 0.79. In the presence of GSH, the bimetallic disulfide-containing complex 3 would be cleaved which was followed by a 8-fold increase in emission intensity of the rhenium(i) moiety. The reaction was found to be specific toward Cys, GSH, and H2S compared to other biothiols. Cell-based assays on complex 1a demonstrated that the addition of GSH to induce cleavage of the disulfide linkage would provide a more cytotoxic agent due to the release of the appended PEG pendant. Cellular localization studies by laser-scanning confocal microscopy in live HeLa cells indicated that complexes 1a-c exhibited punctate staining in the mitochondria.