Impacts of extending the π-conjugation of the 2,2′-biquinoline ligand on the photophysics and reverse saturable absorption of heteroleptic cationic iridium(iii) complexes?

Journal of Materials Chemistry C Pub Date: 2021-10-19 DOI: 10.1039/D1TC03601G

Abstract

Two heteroleptic monocationic Ir(III) complexes bearing 6,6′-bis(7-benzothiazolylfluoren-2-yl)-2,2′-biquinoline as the diimine ligand with different degrees of π-conjugation were synthesized and their photophysics was investigated by spectroscopic techniques and first principles calculations. These complexes possessed two intense absorption bands at 300–380 nm and 380–520 nm in toluene that are predominantly ascribed to the diimine ligand-localized 1π,π* transition and intraligand charge transfer (1ILCT)/1π,π* transitions, respectively, with the latter being mixed with minor 1MLCT (metal-to-ligand charge transfer)/1LLCT (ligand-to-ligand charge transfer) configurations. Both complexes also exhibited a spin-forbidden, very weak 3MLCT/3LLCT/3π,π* absorption band at 520–650 nm. The emission of these complexes appeared in the red spectral region (λem: 640 nm for Ir-1 and 648 nm for Ir-2 in toluene) with a quantum yield of <10% and a lifetime of hundreds of ns, which emanated from the 3ILCT/3π,π* state. The 3ILCT/3π,π* state also gave rise to broad and moderately strong transient absorption (TA) at ca. 480–800 nm. Extending the π-conjugation of the diimine ligand via inserting C[triple bond, length as m-dash]C triplet bonds between the 7-benzothiazolylfluoren-2-yl substituents and 2,2′-biquinoline slightly red-shifted the absorption bands, the emission bands, and the TA bands in Ir-2 compared to those in Ir-1 that lacks the connecting C[triple bond, length as m-dash]C triplet bonds in the diimine ligand. The stronger excited-state absorption with respect to the ground-state absorption at 532 nm led to strong reverse saturable absorption (RSA) for ns laser pulses at this wavelength, with the RSA of Ir-2 being slightly stronger than that of Ir-1, which correlated well with their ratios of the excited-state to ground-state absorption cross sections (σex/σ0). These results suggest that extending the π-conjugation of the 2,2′-biquinoline ligand via incorporating the 7-benzothiazolylfluoren-2-yl substituents retained the broad but weak ground-state absorption at 500–650 nm, meanwhile increased the triplet excited-state lifetimes, which resulted in the much stronger triplet excited-state absorption in this spectral region and strong RSA at 532 nm. Thus, these complexes are promising candidates as broadband reverse saturable absorbers.

Graphical abstract: Impacts of extending the π-conjugation of the 2,2′-biquinoline ligand on the photophysics and reverse saturable absorption of heteroleptic cationic iridium(iii) complexes
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