909019-86-9

Upstream product

• 909019-84-7 C₁₄₂H₂₂₂N₂O₁₀ 
• 629-74-3 hexadec-1-yne 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 752771-80-5 (3,4,5-tris(dodecyloxy)phenyl)methanamine 

Relevant academic research and scientific papers

Coronene charge-transport materials, methods of fabrication thereof, and methods of use thereof

Briefly described, embodiments of this disclosure include coronene charge-transport materials, methods of forming coronene charge-transport materials, and methods of using the coronene charge-transport materials.

Room-temperature discotic liquid-crystalline coronene diimides exhibiting high charge-carrier mobility in air

Six N,N′,5,11-tetrasubstituted coronene-2,3,8,9-tetracarboxydiimides have been synthesised incorporating 3,4,5-tri(n-dodecyloxy)phenyl or 2-(n-decyl)-n-tetradecyl groups in various positions. Differential scanning calorimetry, polarised optical microscopy, and X-ray diffraction indicate that all form columnar discotic mesophases from around room temperature to around 200 °C. Charge-carrier mobility values, which energetic considerations suggest are electron mobility values, have been determined in non-aligned samples cooled from the isotropic melt using the space-charge-limited current technique. The highest mobility, 6.7 cm2 V-1 s-1, was found in N,N′-bis(n-2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecylfluorooctyl)-5,11- bis(3-[{3,4,5-tri(n-dodecyloxy)phenyl}carbonyloxy]-n-propyl)coronene-2,3,8, 9-tetracarboxydiimide, which X-ray diffraction suggests is the most highly ordered of the materials examined.