Two pyrene derivatives having the perylenediimide () or the alky chain () in the middle of molecules were synthesized. Co-assembled supramolecular gels were prepared at different molar ratios of 0.2, 0.5, and 0.8 equiv. of to . By SEM observation, the morphology of co-assembled supramolecular gels changed from spherical nanoparticles to three-dimensional network nanofibers as the ratio of increased. In addition, the pyrene-excimer emission of co-assembled gels increased with increasing concentration of , and was stronger when compared with the condition without or , indicating the formation of pyrene interaction between and . In addition, the sol-gel transition was found to be reversible over repeated measurement by tube inversion method. The rheological properties of co-assembled supramolecular gels were also improved by increasing the ratio of , due to the increased nanoscale flexibility of supramolecular packing by introducing alkyl chain groups through heterogeneous pyrene interaction. These findings suggest that macroscale mechanical strength of co-assembled supramolecular gel was strongly influenced by nanoscale flexibility of the supramolecular packing.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345282PMC
http://dx.doi.org/10.3390/gels6020016DOI Listing

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