Temporally Programmed Hydrogelation of a Short Peptide Charge Transfer Complex
Creating artificial systems that emulate the dynamic behavior of living assemblies remains a central goal in supramolecular chemistry. Here, a charge transfer-driven pH clock-regulated hydrogelation process is presented, arising from the interaction between a pyrene-lysine cysteine tripeptide (PyKC) and a phenylalanine-substituted naphthalene diimide (NDIF). Spectroscopic and structural analyses confirmed the formation of a 1:1 donor-acceptor complex organized through π-π stacking and β-sheet arrangements. The resulting hydrogel forms rapidly under alkaline conditions and exhibits reversible transitions triggered by variations in temperature and pH. Coupling the system with a Tris buffer-glucono-δ-lactone pH clock produces transient hydrogelation with lifetimes precisely tunable by the activator-deactivator ratio. The hydrogel repeatedly assembles and disassembles in synchrony with pH oscillations, maintaining its structural integrity.
Authors
- Rumana Parveen (ORCID: https://orcid.org/0000-0002-9579-8857)
- Subhadeep Sen (ORCID: https://orcid.org/0000-0002-8650-6234)
- Priyam Das
- Debapratim Das (ORCID: https://orcid.org/0000-0003-2295-0966)
- Saurav Das
- Malay Kumar Baroi
Institutions
- Indian Institute of Technology Guwahati (IN)
- Cooch Behar Panchanan Barma University (IN)
- Universidade Estadual do Centro-Oeste (BR)
Publication Details
- Journal
- Langmuir
- Published
- 2026-02-15
- DOI
- https://doi.org/10.1021/acs.langmuir.5c06702
- Citations
- 1
- Primary Topic
- Supramolecular Self-Assembly in Materials
- Type
- article
- Field-Weighted Citation Impact
- 22.64