1621419-18-8

Basic information

• Product Name: 1,3,5-tri{2-cyano-2-[4-(3,4,5-tridodecyloxybenzoylamino)phenyl]-1-ethenyl}phenylbenzene
• CAS NO: 1621419-18-8
• Molecular Weight: 2704.11
• Mol File: 1621419-18-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3,5-tri{2-cyano-2-[4-(3,4,5-tridodecyloxybenzoylamino)phenyl]-1-ethenyl}phenylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tri{2-cyano-2-[4-(3,4,5-tridodecyloxybenzoylamino)phenyl]-1-ethenyl}phenylbenzene(1621419-18-8)
• EPA Substance Registry System: 1,3,5-tri{2-cyano-2-[4-(3,4,5-tridodecyloxybenzoylamino)phenyl]-1-ethenyl}phenylbenzene(1621419-18-8)

Safety Data

• Hazardous Substances Data: 1621419-18-8(Hazardous Substances Data)

Upstream product

• 1621419-14-4 2-[4-(3,4,5-tridodecyloxybenzoylamino)phenyl]-1-acetonitrile 
• 118688-53-2 1,3,5-tris(4-formylphenyl)benzene 

Relevant articles and documents

C3-symmetrical cyano-substituted triphenylbenzenes for organogels and organic nanoparticles with controllable fluorescence and aggregation-induced emission

Fluorescent organic molecules with C3-symmetry consisting of tris{2-cyano-2-[4-(dodecyloxybenzoylamino)phenyl]-1-ethenyl}phenylbenzene (CN-DBAPPBn, n = 1, 2, 3) were synthesized. It was observed that these compounds can spontaneously self-assemble into organogels in many organic solvents. Scanning electron microscopy (SEM), light microscopy, and fluorescence microscopy images of the air-dried gels showed the presence of either heavily entangled amorphous or fibrous structures, or rods. FTIR, UV/Vis absorption, excitation and emission spectra suggest that π-π interactions and H-bonding are the driving forces for the formation of the gel phases. Moreover, spherical or cubic fluorescent nanoparticles based on CN-DBAPPBn were prepared by using a reprecipitation method in a mixture of tetrahydrofuran and water. It is interesting that aggregation-induced emission behavior of CN-DBAPPBn was detected in both the gel phase and in the nanoparticle suspensions. The fluorescent molecular aggregates of CN-DBAPPBn with different architectures and emission properties fabricated by using these self-assembling methods could find potential applications in sensors and optoelectronic devices.