Redox-driven photoselective self-assembly
Self-assembly via non-covalent interactions is key to constructing complex architectures with advanced functionalities. A noncovalent synthetic chemistry approach, akin to organic chemistry, allows stepwise construction with enhanced control. Here, we explore this by coupling Pt(II) complex self-assembly with a redox reaction. Oxidation to Pt(IV) creates a non-emissive monomer that, upon reduction to Pt(II), forms luminescent gels with unique kinetic and thermodynamic pathways. UV irradiation induces Pt(IV) reduction, generating supramolecular fibers with Pt∙∙∙Pt interactions, enhancing photophysical properties and enabling visible light absorption up to 550 nm. This allows photoselective growth, where fibers convert surrounding Pt(IV) to Pt(II), promoting growth over nucleation, as observed via real-time fluorescence microscopy.
Authors
- Piermaria Pinter (ORCID: https://orcid.org/0000-0002-3918-3970)
- Dario R. Alessi (ORCID: https://orcid.org/0000-0002-2140-9185)
- Luca Morgan (ORCID: https://orcid.org/0009-0007-6995-8902)
- Claudia Graiff (ORCID: https://orcid.org/0000-0002-9908-6961)
- Alessandro Aliprandi (ORCID: https://orcid.org/0000-0002-2647-9967)
- Elisa Pelorosso
Institutions
- University of Parma (IT)
- University of Padua (IT)
- St. Elisabeth-Hospital Bochum (DE)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-05-09
- DOI
- https://doi.org/10.1038/s41467-025-58890-4
- Citations
- 4
- Primary Topic
- Supramolecular Self-Assembly in Materials
- Type
- article
- Field-Weighted Citation Impact
- 2.39
Funders
- Dipartimenti di Eccellenza
- European Commission
- Ministero dell’Istruzione, dell’Università e della Ricerca