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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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http://dx.doi.org/10.1002/chem.202500866 | DOI Listing |
Int J Biol Macromol
September 2025
Department of Chemical Engineering, Institute of Chemical Technology, Matunga (E), Mumbai, 400019, India. Electronic address:
Integrating multi-enzyme systems within metal-organic frameworks (MOFs) has garnered significant attention in biocatalysis due to their tunable structural properties and ability to enhance enzyme performance in cascade reactions. The unique features of MOFs, such as well-defined pore apertures, tailorable compositions, and high loading capacity, facilitate the design of robust multi-enzyme bio-composites with enhanced recyclability and specificity. This review explores systematic approaches for the compartmentalization and positional co-immobilization of multiple enzymes within MOFs, focusing on two key strategies: (i) layer-by-layer assembly and (ii) pore-engineered compartmentalization.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, China. Electronic address:
Precise control of particle size, pore size distribution, and carbon layer spacing under green and low-energy conditions is critical for developing advanced carbon electrodes for supercapacitors and sodium-ion batteries (SIBs). Herein, we proposed a new strategy to prepare an MgAl bimetallic metal-organic framework (MOF) via a pre-ionization strategy, effectively avoiding harsh conditions and using organic solvents in hydrothermal synthesis. By fine-tuning the Mg/Al ratio and pyrolysis conditions, the particle size, pore size distribution and carbon layer spacing of rod porous carbon (RPC) were precisely adjusted.
View Article and Find Full Text PDFLangmuir
September 2025
School of Resources Engineering, Xi'an University of Architecture & Technology, Xi'an, Shaanxi 710055, China.
The use of highly flammable materials such as foams, resins, and plastics has led to an increase in the frequency and severity of urban fires worldwide. To address this issue, this study developed a high-specific-surface-area mesoporous metal-organic framework (Fe-MOFs) with heat trapping and smoke adsorption. The Fe-MOFs, zinc tailings (ZTs), piperazine pyrophosphate (PAPP), and sodium lignosulfonate (LS) were used to modify rigid polyurethane foam (RPUF).
View Article and Find Full Text PDFRSC Adv
August 2025
School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology 1037 Luoyu Road, Hongshan District Wuhan 430074 China.
The post-synthesis of metal-organic frameworks (MOFs) plays a valuable role in enhancing their properties and functionalities. Herein a pillared layer mixed ligand metal-organic framework, derived (DMOFs) from 2-aminoterephthalic acid (BDC-NH) as an -donor and 1,4-diazabicyclo[2.2.
View Article and Find Full Text PDFACS Nano
September 2025
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430079, P. R. China.
Burns complicated by antibiotic-resistant bacterial infections present a formidable clinical challenge, characterized by key pathological processes, including pathogen colonization, chronic inflammatory responses, and excessive accumulation of reactive oxygen species (ROS). Photocatalytic metal-organic frameworks (MOFs) have emerged as a promising nonantibiotic strategy against antibiotic-resistant bacterial infections. However, the ROS generated by MOF-based photocatalysis is often insufficient for effective antibacterial activity, while excessive ROS may induce tissue injury.
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