Synthesis and Photophysical Properties of a Series of Dimeric Indium Quinolinates
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Published on: May 7, 2019
Sang Woo Kwak1, Ju Hyun Hong2, Sanghun Lee1
1Department of Chemistry, Chungbuk National University, Cheongju 28644, Korea.
Abstract:
A novel class of quinolinol-based dimeric indium complexes (1-6) was synthesized and characterized using 1H and 13C(1H) NMR spectroscopy and elemental analysis. Compounds 1-6 exhibited typical low-energy absorption bands assignable to quinolinol-centered π-π* charge transfer (CT) transition. The emission spectra of 1-6 exhibited slight bathochromic shifts with increasing solvent polarity (p-xylene < tetrahydrofuran (THF) < dichloromethane (DCM)). The emission bands also showed a gradual redshift, with an increase in the electron-donating effect of substituents at the C5 position of the quinoline groups. The absolute emission quantum yields (ΦPL) of compounds 1 (11.2% in THF and 17.2% in film) and 4 (17.8% in THF and 36.2% in film) with methyl substituents at the C5 position of the quinoline moieties were higher than those of the indium complexes with other substituents.
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