Photophysical Properties and Photobiological Activities of Ruthenium(II) Complexes Bearing π-Expansive Cyclometalating Ligands with Thienyl Groups.

A new family of cyclometalated ruthenium(II) complexes [Ru(N^N)(C^N)] derived from the π-extended benzo[]imidazo[4,5-]quinolone ligand appended with thienyl groups ( = 1-4, compounds -) was prepared and its members were characterized for their chemical, photophysical, and photobiological properties. The lipophilicities of -, determined as octanol-water partition coefficients (log ), were positive and increased with the number of thienyl units. The absorption and emission bands of the C^N compounds were red-shifted by up to 200 nm relative to the analogous Ru(II) diimine systems. All of the complexes exhibited dual emission with the intraligand fluorescence (IL, C^N-based) shifting to lower energies with increasing and the metal-to-ligand charge transfer phosphorescence (MLCT, N^N-based) remaining unchanged. Compounds - exhibited excited state absorption (ESA) profiles consistent with lowest-lying MLCT states when probed by nanosecond transient absorption (TA) spectroscopy with 532 nm excitation and had contributions from IL(C^N) states with 355 nm excitation. These assignments were supported by the lifetimes observed (<10 ns for the IL states and around 20 ns for the MLCT states) as well as a noticeable ESA for with 355 nm excitation that did not occur with 532 nm excitation. Compound was the only member of the family with two MLCT emissive lifetimes (15, 110 ns), and the TA spectra collected with both 355 and 532 nm excitation was assigned to the IL state, which was corroborated by its 4-6 μs lifetime. The ESA for had a rise time of approximately 10 ns and an initial decay of 110 ns, which suggests a possible MLCT-IL excited state equilibrium that results in delayed emission from the MLCT state. Compound was nontoxic toward human skin melanoma cells (SKMEL28) in the dark (EC = >300 μM); - were cytotoxic and yielded EC values between 1 and 20 μM. The photocytotoxicites with visible light ranged from 87 nM with a phototherapeutic index (PI) of 13 for to approximately 1 μM (PI = >267) for . With red light, EC values varied from 270 nM (PI = 21) for to 12 μM for (PI = >25). The larger PIs for , especially with visible light, were attributed to the much lower dark cytotoxicity for this compound. Because the dark cytotoxicity contributes substantially to the observed photocytotoxicity for -, it was not possible to assess whether the IL state of led to a much more potent phototoxic mechanism in the absence of dark toxicity. There was no stark contrast in cellular uptake and accumulation by laser scanning confocal and differential interference contrast microscopy to explain the large differences in dark toxicities between - and . Nevertheless, the study highlights a new family of Ru(II) C^N complexes where π-conjugation beyond a certain point results in low dark cytotoxicity with high photocytotoxicity, opposing the notion that cyclometalated Ru(II) systems are too toxic to be phototherapeutic agents.