Helical Stacking Tuned by Alkoxy Side Chains in π-Conjugated Triphenylbenzene Discotic Derivatives

We report on the synthesis and self‐assembly of a new series of discotic molecules containing triphenylbenzene as the core and alkoxy side chain with varying length. It was found that compounds 3 a–c, 4 b and 5 b could form stable gels in several apolar solvents. Transmission electron microscopy (TEM) images revealed that their morphologies were very different for the different alkoxy‐substituted organogels. In toluene or hexane, 3 b and 3 c resulted in both left‐ and right‐handed helical fibers, whereas 3 a resulted in straight rigid fibers; 4 b and 5 b resulted in most straight fibers with a few twisted fibers. The results from FT‐IR and UV/Vis absorption spectroscopy indicated that the hydrogen bonding and π–π interactions were the main driving forces for the formation of the self‐assembled gels. Further detailed analysis of their aggregation modes were conducted by UV‐visible absorption spectra and X‐ray diffraction (XRD) measurements. Based on these findings, the influence of these peripheral alkoxy substituents on the gel formation and the aggregation mode were discussed. The special enhanced fluorescent emissions, which resulted from aggregation, were also found in the gel phase. Both left‐ and right‐handed helical fibers such as depicted were obtained from π‐conjugated triphenylbenzene discotic molecules. The morphologies and microstructures of the self‐assemblies could be tuned by the peripheral substituted alkoxy side chains.