Azomethine liquid crystals (LCs), constituted by symmetric and asymmetric bithiophene or fluorene units as chromophores, were designed and synthesised. Their thermotropic behaviour was investigated using optical microscopy, differential scanning calorimetry, and wide angle X-ray diffraction. A lowering of transition temperatures was obtained by the introduction of the lateral methyl group as compared with unsubstituted compounds. The observed LC phases possess the classical textures of calamitic LCs. The optical properties of the target compounds were evaluated, both in solution and in solid state. A blue fluorescence was observed for fluorene containing compounds and a green fluorescence was observed for analogous bithiophene containing compounds. The introduction of a methyl lateral group onto the aromatic rings led to a remarkable increase in the solution emission properties.
Synthesis and liquid crystalline properties of new azomethine derivatives exhibiting luminescent properties
Destri S;Porzio W;Bertini F
2009
Abstract
Azomethine liquid crystals (LCs), constituted by symmetric and asymmetric bithiophene or fluorene units as chromophores, were designed and synthesised. Their thermotropic behaviour was investigated using optical microscopy, differential scanning calorimetry, and wide angle X-ray diffraction. A lowering of transition temperatures was obtained by the introduction of the lateral methyl group as compared with unsubstituted compounds. The observed LC phases possess the classical textures of calamitic LCs. The optical properties of the target compounds were evaluated, both in solution and in solid state. A blue fluorescence was observed for fluorene containing compounds and a green fluorescence was observed for analogous bithiophene containing compounds. The introduction of a methyl lateral group onto the aromatic rings led to a remarkable increase in the solution emission properties.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
