ArticleNature chemistry2025
Introducing metal-sulfur active sites in metal-organic frameworks via post-synthetic modification for hydrogenation catalysis.
Article in Nature chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed.
- Suppression of Peierls Instability in a Metal-Halide Porous Framework.Angewandte Chemie (International ed. in English) · 2026Article
- Photocatalytic Transfer Hydrogenation Using Plastic Hydrolysates as Hydrogen Donor.Angewandte Chemie (International ed. in English) · 2026Article
- Defect-Engineered MOF-808-SOMolecules (Basel, Switzerland) · 2026Article
- Reprogramming Porosity: The Synthetic Evolution of Pore Engineering in Metal-Organic Frameworks.ACS materials letters · 2026Review
- Harnessing the structural evolution of metal-organic frameworks under electrocatalytic conditions.Communications chemistry · 2025Review
Corrections and comments
- Erratum issued
Authors and funding
24 authors.
Funding
Abstract
Metal-sulfur active sites play a central role in catalytic processes such as hydrogenation and dehydrogenation, yet the majority of active sites in these compounds reside on the surfaces and edges of catalyst particles, limiting overall efficiency. Here we present a strategy to embed metal-sulfur active sites into metal-organic frameworks (MOFs) by converting bridging or terminal chloride ligands into hydroxide and subsequently into sulfide groups through post-synthetic modification. We apply this method to two representative MOF families: one featuring one-dimensional metal-chloride chains and another containing discrete multinuclear metal clusters. Crystallographic and spectroscopic analyses confirm structural integrity and sulfide incorporation, and the transformation is monitored by in situ total scattering methods. The sulfided MOFs display enhanced catalytic activity in the selective hydrogenation of nitroarenes using molecular hydrogen. Density functional theory calculations indicate that sulfur incorporation promotes homolytic metal-ligand bond cleavage and facilitates H
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40707779What OpenQuestion holds
Registered trials
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