RESUMO
The novel terthiophene (3T) oligomer 6 and a series of cationic Ir(III) bis-cyclometalates [Ir(C^N)(2)(N^N)]PF(6) 9-12 were prepared. The synthesis, characterization, electrochemical, and photophysical properties are reported. The cyclometalating ligands (C^N) are 2-phenylpyridinato (ppy) or the 3T oligomer (3T-ppy), asymmetrically capped in the 5 and 5" positions with the ppy and mesityl groups. The diimine ligands (N^N) are 2,2'-bipyridine (bpy) or 4-NO(2)-bipyridine (4-NO(2)-bpy). Hybrid metal-organic complexes 11 and 12 bear 3T-pendants ligated through the ppy cap, 10 and 12 contain NO(2) functionalized diimines, whereas 9 contains neither. Structural characterization of 10 by single crystal X-ray diffraction confirms the presence of the NO(2) substituent and pseudo-octahedral coordination geometry about the Ir(III) ion. Cyclic voltammetry highlights the large electron withdrawing effect of the NO(2) substituent, providing an 850 mV shift toward lower potentials for the first diimine centered reduction of 10 and 12. Strong overlap of the intense π â π* absorptions of the 3T-pendants with Ir(III) charge transfer bands is evident in complexes of 11 and 12, precluding the possibility for selective excitation of either chromophore. Photoexcitation (λ(ex) = 400 nm) of the series affords strong luminescence from the 3T oligomer 6 and the unsubstituted 9, with φ(em) = 0.11. In stark contrast the NO(2) and 3T functionalized complexes 10-12 display near total quenching of luminescence. Computations of the ground and excited state electronic structure using density functional theory (DFT) and time-dependent DFT (TD-DFT) indicate that both the NO(2) and 3T substituents play an important role in excited state deactivation of complexes 10-12. A substantial electronic contribution of the NO(2) substituent results in stabilization of the diimine based molecular orbital (MO) and offers an efficient nonradiative decay pathway for the excited state. Spin-orbit coupling effects of the Ir(III) ion lead to efficient population of the low lying, nonluminescent, triplet states centered on the 3T-pendants.
RESUMO
Photophysical data for a series of end substitued 3',4'-dibutyl-2,2':5',2''-terthiophenes are reported. Static absorption and fluorescence, quantum yields, time-resolved fluorescence, and time- and frequency-resolved pump-probe spectra are applied to investigate excited state relaxation in bromo, nitro, and tricyanovinyl substituted species in a variety of solvents. The effect of solvent polarizability and end-group substitution is discussed in the context of charge transfer in the excited state and its impact on nonradiative decay rates. In solution at room temperature, both symmetric and asymmetric addition of electron withdrawing end groups generate an excited state with substantial charge transfer character. Solvent polarizability has a significant influence on the excited state dynamics in the charge transfer compounds. Examples include a 20-fold reduction in the intersystem crossing rate going from hexane to toluene and an order of magnitude increase in the internal conversion rate between toluene and acetone. The results demonstrate that the impact of the substituents on intramolecular charge transfer, and the resulting amplification of the interactions between the excited state(s) and the local molecular environment, can dramatically change the excited state relaxation dynamics in substituted terthiophenes.