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Abstract
The seven
N
-phthalimide derivatives substituted with the amine group at the 3-C position in the phenylene ring were synthesized. The effect of
N
-substituent chemical structure was investigated. The thermal, electrochemical and optical studies were performed and supported by the density functional theory calculations (DFT). The electrochemical investigations of the synthesized low-molecular phthalimides revealed the one oxidation and reduction process with the HOMO energy level under − 5.81 eV and energy-band gap below 3 eV. The
N
-phthalimide derivatives were emitted light in a blue spectral region in solutions (in polar and non-polar) with the quantum yield between 2 and 68%, dependent on the substituent at the nitrogen atom, solvent and concentration. The
N
-phthalimide derivatives were emissive also in a solid state as a thin film and powder. They were tested as a component of the active layer with PVK:PBD matrix and as an independent active layer in the organic light-emitting diodes. The registered electroluminescence spectra exhibited the maximum emission band in the 469–505 nm range, confirming the possibility of using
N
-phthalimides with PVK:PBD matrix as the blue emitters.