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Here, an ultra-highly active Ni-MOF-5 catalyst with high Ni loading for ethylene dimerization is reported. The Ni-MOF-5 catalysts are synthesized by a facile one-pot co-precipitation method at room temperature, where Ni replaces Zn in MOF-5. Unlike Zn with tetrahedral coordination in MOF-5, Ni is coordinated with extra solvent molecules except for four-oxygen from the framework. After removing coordinated solvent molecules, Ni-MOF-5 achieves an ethylene turnover frequency of 352 000 h , corresponding to 9040 g of product per gram of catalyst per hour, at 35 °C and 50 bar, far exceeding the activities of all reported heterogeneous catalysts. The high Ni loading and full exposure structure account for the excellent catalytic performance. Isotope labeling experiments reveal that the catalytic process follows the Cossee-Arlman mechanism, rationalizing the high activity and selectivity of the catalyst. These results demonstrate that Ni-MOF-5 catalysts are very promising for industrial catalytic ethylene dimerization.
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http://dx.doi.org/10.1002/smll.202301235 | DOI Listing |
Dalton Trans
September 2025
ICGM, Univ. Montpellier, CNRS, ENSCM, 34090 Montpellier, France.
The synthesis and structural characterisation of a series of alkaline earth -octaphenylmetallocenes (Mg, Ca, Sr, Ba) bearing an ethylene bridge are described. The complexes [AE(CPhCH)(thf)] (AE = Mg (1), Ca (2) = 1; AE = Sr (3), Ba (4), = 2) were obtained through reductive dimerisation of 1,2,3,4-tetraphenylfulvene, facilitated by zero-valent metals and fully characterised by NMR spectroscopy. Single-crystal XRD studies reveal distinct binding differences of the Cp ligands to Mg in complex 1 compared to the heavier analogues (η η).
View Article and Find Full Text PDFCryst Growth Des
August 2025
Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, 10000 Zagreb, Croatia.
In this work, we synthesized three novel 4-iodotetrafluorophenoxy-azobenzene ethers, which contain different substituents (X = -H, -Cl, -CN) on the opposite side of the molecule in relation to the perhalogenated moiety carrying the iodine atom. To explore the halogen bond donor potential of the prepared compounds, we performed cocrystal screening with a series of nitrogen-containing acceptors: 1,4-diazabicyclo[2.2.
View Article and Find Full Text PDFBioresour Technol
August 2025
BOKU University, Institute of Environmental Biotechnology, Department of Agricultural Sciences, Tulln an Der Donau, Austria. Electronic address:
This study investigates enzymatic hydrolysis of four novel polyesters (REPolymers) with different structures based on terephthalic acid, ethylene glycol, glutaric acid, and decanediol. These polyesters were synthesized from PET building blocks and bio-based monomers. A hydrolase from Rhizobacter sp.
View Article and Find Full Text PDFAcc Chem Res
September 2025
Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
ConspectusPolyolefins are by far the most ubiquitous industrially produced polymers and are primarily produced by early transition metal catalysts. These catalysts are not functional group tolerant, and copolymerization of ethylene and polar vinyl monomers is quite challenging. Furthermore, early metal catalysts convert ethylene to linear polyethylene, and introduction of branches requires addition of comonomers.
View Article and Find Full Text PDFSoft Matter
September 2025
Department of Materials Science and Engineering, Indian Institute of Technology Delhi, New Delhi-110016, India.
It is being increasingly recognized that a comprehensive understanding of protein folding and aggregation requires accounting for the crowded milieu. Such a complex milieu offers a variety of soft, non-specific interactions along with the crowder volume exclusion effects that can modulate the hydration and protein aggregation processes. A clear understanding of the interplay of these effects is still lacking.
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