Demonstrates enhanced covalent functionalization of ZIF-8 nanoparticles, suggesting wider application in various fields.
High Resolution Image Download MS PowerPoint Slide Zeolitic imidazolate framework-8 (ZIF-8) is a widely studied metal–organic framework for a range of applications. However, its limited availability of reactive surface groups restricts controlled covalent functionalization. Here, we introduce amino (–NH 2 ), aldehyde (–CHO), and carboxylate (–COOH) functionalities onto nanosized ZIF-8 via solvent-assisted ligand exchange while preserving crystallinity and morphology. The degree of ligand exchange can be tuned by adjusting the reaction time, reaching values between 4 and 15%, as quantified by NMR spectroscopy. The chemical accessibility of the introduced groups is demonstrated through covalent conjugation reactions, including fluorescein labeling and carbodiimide-mediated amide formation. This approach establishes a versatile platform for equipping ZIF-8 nanoparticles with reactive surface functionalities, enabling modular postsynthetic modification for applications in catalysis, sensing, biomedicine, and beyond.
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Stammler et al. (2026) studied this question.
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