ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025
A Copper(I) Catenane Decorated Metal-Organic Layer as a Heterogenous Catalyst for Dehydrogenative Cross-Coupling.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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
1 citing paper in PubMed.
- Structural Dependence of Catenand Effect: Thermodynamic and Kinetic Modulation of Catenane Coordination Properties via Ring-size and Exocyclic Substituent Variation.Angewandte Chemie (International ed. in English) · 2025Article
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8 authors.
Funding
Abstract
While earth-abundant metals are green and sustainable alternatives to precious metals for catalytic chemical conversions, the fast ligand exchange involving most of the base metals renders their development into robust, reusable catalysts very challenging. Described in this work is a new type of heterogeneous catalyst derived from a 2D metal-organic layer (MOL) grafted with catenane-coordinated Cu(I) complexes. In addition to the good substrate accessibility, easy functionalization, and other favorable features due to the MOL support, the mechanical bond in the anchored catenane ligands also represents a new mechanism to dynamically confine the coordination environment and kinetically stabilize the coordinated Cu(I) to give a well-defined, active yet stable heterogeneous catalyst. Pilot catalytic studies using a model dehydrogenative C─O cross-coupling reaction showed that the Cu(I) catenane-grafted MOL led to exclusive formation of the C─O coupled product, whereas control catalysis using a similar Cu(I) catalyst supported by non-interlocked macrocyclic ligands was found to also give a C─C coupled by-product, whose formation was found to be mediated by the uncontrolled oxidation of the Cu(I) to Cu(II), highlighting the distinctive roles and untapped potential of the catenane coordination in developing base metal-derived catalysts for challenging catalytic conditions.
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