Mono-nuclear fac-Re(CO)(3)(ph(2)phen)(4,4'-bpy)(+) and di-nuclear (ph(2)phen)(CO)(3)Re(4,4'-bpy)Re(ph(2)phen) (CO)(3)(2+) complexes, ph(2)phen = 4,7-diphenyl-1,10-phenanthroline and 4,4'-bpy = 4,4'-bipyridine, were synthesized and characterized by H-1 NMR, UV-visible and FT-IR spectroscopy. Also, their photophysical properties were investigated using steady-state and time-resolved emission spectroscopy. Both complexes showed UV absorption assigned to intraligand, (1)ILph(2)phen, and metal-to-ligand charge transfer, (MLCTRe -> ph2phen)-M-1, transitions, and typical (MLCTRe -> ph2phen)-M-3 emission (phi= 0.360 and tau = 3.81 mu s; phi = 0.177 and tau = 1.90 mu s for mono- and di-nuclear, respectively). Additionally, the luminescence of these complexes is quenched by hydroquinone with approximately 4 x 10(9) L mol(-1) s(-1) rate constant for the bimolecular excited state, k(q). The Stern-Volmer constants, K-SV, determined by the emission intensity and lifetime showed excellent correlation, which is indicative of the dynamic quenching. The similarity of the bimolecular rate constants between the two complexes implies that the photoinduced electron transfer is the main pathway with a very small (or no) influence of the proton transfer step. The results provide additional insight into the role of the protonable nitrogen atom in the photophysical properties of rhenium(I) complexes, using a dyad architecture.
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