Carbazole-Appended Salen–Indium Conjugate Systems:Synthesis and Enhanced Luminescence Efficiency

Novel carbazole-conjugated salen–In complexes (Cz1 and Cz2) were prepared and fully characterized by 1H and 13C NMR spectroscopy, elemental analysis, and high-resolution mass spectrometry. The major low-energy absorption bands at λabs = 342 nm for Cz1 and 391 nm for Cz2, respectively, are assigned to typical intramolecular charge transfer (ICT) transitions between the carbazole unit and the salen–In center. The solvatochromism effects in various organic solvents and their large Stokes shift distinctly supported the ICT nature. The photoluminescent spectra of Cz1 and Cz2 showed broad emission bands are centered at 459 nm (blue, λex = 354 nm) and 507 nm (green, λex = 396 nm) in THF, respectively, which are typical feature of CT transitions. In particular, Cz1 showed 8-fold enhanced quantum efficiency relative to that of Cz2, at least 10-fold higher than those of the carbazole-free salen–In complexes. Such enhanced luminescence efficiency of Cz1 originated from efficient radiative decay based on the ICT tran...