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Blue-emissive two-component supergelator with aggregation-induced enhanced emission. | LitMetric

AI Article Synopsis

  • Two-component organogels have significant advantages over one-component gels, but they are difficult to design effectively.
  • Researchers developed a new class of supergelators using acid-functionalized TPE dendrons and alkylated melamine, which do not gel individually but create a gel when combined.
  • The gelation is driven by strong π-π stacking interactions, leading to intense fluorescence and excellent elasticity, showcasing the potential for creating advanced materials with unique properties not found in the original components.

Article Abstract

Two-component organogels offer several advantages over one-component gels, but their design is highly challenging. Hence, it is extremely important to design new approaches for the crafting of two-component organogels with interesting optical and mechanical properties. Herein, we report the design of a new class of two-component supergelators obtained from the assembly between acid functionalized tetraphenylethylene (TPE)-based dendrons and alkylated melamine. No gelation behaviour is observed for the individual components, but interestingly, remarkable gelation behaviour is observed for their hydrogen-bonded complex. The primary driving force responsible for the gelation is the strong π-π stacking interaction of TPE units. Because of the strong π-stacking of TPEs in the gel state, the C(sp)-C(sp) bond rotation of the TPE segment is completely arrested in the gel state, which results in intense fluorescence emission of the gels. Furthermore, excellent elastic response is observed for the gels as evident from their high storage modulus compared to loss modulus values. Our results clearly demonstrate that by the appropriate selection of the molecular components, this approach can be applied for the creation of functional nanomaterials with emergent properties absent in the individual blocks.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033671PMC
http://dx.doi.org/10.1039/d1ra03751jDOI Listing

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