Unsymmetrical and symmetrical azomethines were obtained using the condensation reaction of diamino-thiophene-3,4 dicarboxylic acid diethyl ester with 4-(1-pyrrolidino)benzaldehyde, fluorene-2-carboxaldehyde, 1-methylindole-3-carboxaldehyde, and benzothiazole-2-carboxaldehyde. Their thermal, optical, and electrochemical properties were investigated, and the results were supported by calculations using the density functional theory. The studied compounds melted in the range of 170-260 degrees C and can be converted into amorphous materials with high glass transition temperatures between 76 and 135 degrees C. They were thermally stable up to 220-300 degrees C. All imines were electrochemically active and exhibited low energy band gaps below 2 eV (except for one imine with E-g = 2.39 eV) determined on the basis of cyclic voltammetry. Most of the azomethines were emissive in solution and in the solid state. Some of them showed both S-1 (first excited state) emission and S-2 (second excited state) emission or only fluorescence from higher excited state, which is first time observed for azomethines. The imine with the most promising properties was tested in a light-emitting diode, and its ability for emission of light under external voltage was demonstrated.