Abstract

The photophysical properties of a series of tris-cyclometalated Ir(III) complexes bearing oligofluorene-substituted 2-phenylpyridine (ppy) and/or 1-phenylisoquinoline (piq) ligands were studied at both room temperature and 77 K, for delineating the oligomer-substitution effects on the photophysics in such metal-complex-containing conjugated oligomers/polymers. Unique temperature dependence was observed with the triplet excited-state lifetime of the studied oligomers. Molecules having one of the three ppy ligands substituted with an oligofluorenyl group at varied positions exhibited two distinct types of phosphorescing behaviors. When the oligoflurene group was coupled to ppy in a conjugative fashion (i.e., at 5- or 4′- position), the complexes appeared to emit from a 3MLCT-dominated state perturbed by LC transition, as evidenced by the relatively short lifetimes of phosphorescence as well as hypsochromic shift upon lowering the temperature. Surprisingly, even shorter triplet lifetimes were detected at 77 ...

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