Filtern
Dokumenttyp
- Zeitschriftenartikel (1)
- Preprint (1)
Sprache
- Englisch (2)
Schlagworte
- Black phosphorus (2)
- Advanced surface characterization (1)
- Antiviral materials (1)
- Biodegradability (1)
- Bonding motifs (1)
- Covalent functionalization (1)
- DFT calculations (1)
- Functionalization (1)
- Raman spectroscopy (1)
- SEM/EDX (1)
Organisationseinheit der BAM
Abteilungsübergreifende Publikation
- nein (2)
Scalable covalently functionalized black phosphorus hybrids for broadspectrum virucidal activity
(2025)
At the onset of viral outbreaks, broad-spectrum antiviral materials are crucial before specific therapeutics become available. We report scalable, biodegradable black phosphorus (BP) hybrids that provide mutation-resilient virucidal protection. BP sheets, produced via an optimized mechanochemical process, are covalently functionalized with 2-azido-4,6-dichloro- 1,3,5-triazine to form P=N bonds. Fucoidan, a sulfated polysaccharide with intrinsic antiviral activity, and hydrophobic chains are then incorporated to achieve irreversible viral deactivation. The material exhibits strong antiviral inhibition and complete virucidal activity against multiple viruses, including recent severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants. It maintains high biocompatibility, remains effective against viral mutations, and is shelf stable for at least five month. The combination of biodegradability, scalable synthesis, and synergistic antiviral and virucidal mechanisms establishes BP-conjugates as a new class of highly efficient antivirals. They offer a broad spectrum antiviral solutions that could bridge the gap between antiviral medicines and general antiseptics.
Controllable covalent surface functionalization of black phosphorus (BP) remains a central challenge in the development of 2D phosphorus‐based materials. Here, we report a scalable route to synthesize biodegradable BP‐polymer hybrids and establish optimal conditions for BP production, exfoliation, and covalent modification. BP sheets, produced via optimized mechanochemical and exfoliation processes, are covalently functionalized with 2‐azido‐4,6‐dichloro‐1,3,5‐triazine via a nitrene‐mediated [2+1] cycloaddition. The reaction yields a P‐N bond, verified by advanced surface analyses and density functional theory (DFT) calculations. The conjugated triazine groups enable subsequent nucleophilic aromatic substitution reactions, providing a versatile platform for controlled post‐modification of BP surface. This covalent functionalization strategy addresses key limitations in BP surface chemistry and provides a route toward biodegradable phosphorus‐based hybrid materials. As a representative example, functionalization with linear polyglycerol sulfate produces BP‐polymer conjugates that inhibit respiratory syncytial virus (RSV) and herpes simplex virus 1 (HSV‐1) at low‐microgram‐per‐milliliter concentrations.