Abstract
The bottom-up approach exploits simple building blocks to generate new materials with desired physical and chemical characteristics. Here, we combine two bottom-up routes that occur under mild conditions, self-assembly and sol-gel synthesis, to program the shape and structure of materials. While self-assembly occurs through non-covalent interactions, sol-gel synthesis involves forming covalent bonds. As a proof of concept, we chose the self-assembled peptide Phe-Phe and its fluorinated analogue Phe(4-F)-Phe(4-F) to template the sol-gel process. These peptides were silylated to allow their self-mineralization. Scanning electron microscopy and atomic force microscope analysis revealed the formation of rod-shaped structures for the silylated Phe-Phe while spherical particles were formed by its fluorinated analogue. The size of the particles ranges from nano to micron scale. Fourier transform infrared spectrometry suggested the presence of parallel β-sheet secondary structure and siloxane bond formation that can stabilize these structures. Overall this approach can be adopted for other self-assembled peptides for generating new materials using a bottom-up approach.
| Original language | English |
|---|---|
| Pages (from-to) | 204-214 |
| Number of pages | 11 |
| Journal | Faraday Discussions |
| Volume | 260 |
| DOIs | |
| State | Published - 28 Aug 2025 |
| Externally published | Yes |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry