Artigo do professor Thiago Cazatti, do FIMAT, publicado na Eur. J. Inorg. Chem. 2019, 2247–2257, é capa da revista
New Boron(III) Blue Emitters for All‐Solution Processed OLEDs: Molecular Design Assisted by Theoretical Modeling
Cristian A. M. Salla, Jéssica Teixeira dos Santos, Giliandro Farias,
Adailton J. Bortoluzi, Sergio F. Curcio, Thiago Cazati, Róbert Izsák, Frank Neese,[d]
Bernardo de Souza, and Ivan H. Bechtold
Luminescent boron(III) complexes have recently been employed as emitters in organic light‐emitting diodes (OLEDs) with reasonable success. They are easy to prepare and sufficiently stable to be used in such devices, being of great interest as a simple molecular emissive layer. Although emitters for this class with all colors have already been reported, highly efficient and stable blue emitters for applications in solution processed devices still pose a challenge. Here, we report the design, synthesis, and characterization of new boron complexes based on the 2‐(benzothiazol‐2‐yl)phenol ligand (HBT), with different donor and acceptor groups responsible for modulating the emission properties, from blue to red. The molecular design was assisted by calculations using our newly developed formalism, where we demonstrate that the absorption and fluorescence spectra can be successfully predicted, which is a powerful technique to evaluate molecular photophysical properties prior to synthesis. In addition, density functional theory (DFT) enables us to understand the molecular and electronic structure of the molecules in greater detail. The molecules studied here presented fluorescence efficiencies as high as Φ = 0.88 and all solution processed OLEDs were prepared and characterized under an ambient atmosphere, after dispersion in the emitting layer. Surprisingly, even considering these rather simple experimental conditions, the blue emitters displayed superior properties compared to those in the present literature, in particular with respect to the stability of the current efficiency.