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Organogels of FmocFF: Exploring the Solvent-Dependent Gelmorphic Behavior
Basanta Saikia1, Dong Chen1, Yovan de Coene2
1Department of Chemistry, Molecular Imaging and Photonics, KULAK-KU Leuven, E. Sabbelaan 53, 8500 Kortrijk, Belgium.
9-fluorenyl methoxycarbonyl-phenylalanine (FmocFF) forms robust organogels in various solvents. Gel properties depend on solvent choice, crystallinity, and morphology, revealed by rheology and in situ SHG microscopy.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Organic Chemistry
Background:
- 9-fluorenyl methoxycarbonyl-phenylalanine (FmocFF) is a well-studied low-molecular-weight hydrogelator.
- The organogelation potential of FmocFF remains underexplored despite extensive hydrogel research.
Purpose of the Study:
- To systematically investigate the formation and properties of FmocFF-based organogels across a spectrum of organic solvents.
- To elucidate the factors influencing gelmorphic behavior, mechanical strength, and structural characteristics of FmocFF organogels.
Main Methods:
- Systematic exploration of FmocFF organogelation in diverse organic solvents.
- Rheological measurements to assess mechanical strength.
- In situ second-harmonic generation (SHG) microscopy for native gel structure analysis.
Main Results:
- FmocFF demonstrates robust organogelation capabilities across various organic solvents.
- Organogels exhibit diverse gel morphologies and degrees of crystallinity, influenced by the solvent.
- Mechanical properties and structure are significantly affected by both solvent-solute interactions and the degree of crystallinity.
Conclusions:
- FmocFF is a versatile organogeltor with tunable properties based on solvent selection.
- Crystallinity emerges as a critical factor, alongside solvent-solute interactions, in dictating FmocFF organogel structure and mechanical performance.
- In situ SHG microscopy provides valuable insights into the native state of organogel structures.
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