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Designing composite catalysts that harness the strengths of individual components while mitigating their limitations is a fascinating yet challenging task in catalyst engineering. In this study, we aimed to enhance the catalytic performance by anchoring ZIF-67 nanoparticles of precise sizes onto lamella Si-MWW zeolite surfaces through a stepwise regrowth process. Co ions were initially grafted onto the zeolite surface using ultrasonication, followed by a seed-assisted secondary growth method. Si-MWW proved to be the ideal zeolite support due to its thin layered structure, large external surface area and substantial lateral dimensions. The abundant Si-OH groups on its surface played a crucial role in securely binding Co ions, limiting size growth and preventing undesirable ZIF-67 aggregation. The resulting ZIF-67/MWW composite with finely dispersed nano-scale ZIF-67 particles exhibited a remarkable catalytic performance and stability in the aldol condensation reactions involving acetone and various aldehydes. This approach holds promise for designing MOF/zeolite composite catalysts.
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http://dx.doi.org/10.1039/d4dt00288a | DOI Listing |
RSC Adv
August 2025
Natural and Medical Sciences Research Center, University of Nizwa P.O. Box 33, Postal Code 616, Birkat Al Mauz Nizwa Sultanate of Oman.
A new series of dihydronaphthalen-1(2)-one derivatives were synthesized in high yields starting from commercially available 3,5,5-trimethylcyclohex-2-en-1-one 1a, aromatic aldehydes 2, and diethyl acetylenedicarboxylate. Reaction of 1a with the aldehydes produced the respective dienones 3, which could cycloadd to dialkyl acetylenedicarboxylate, either stepwise or , under aqueous/organocatalyzed (DMAP) conditions. The respective adducts 4, were produced efficiently a Diels-Alder-double bond isomerization-oxidative aromatization sequence and were characterized based on the analysis of their H and C NMR spectra.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
We previously reported that molecules containing two cyclic hydrazide units connected by a polymethylene linker could catalyze aldol condensations via a bifunctional mechanism. One hydrazide apparently provides nucleophilic activation, via enamine formation, while the other provides electrophilic activation, via iminium formation. Here, we ask whether catalytic efficacy can be enhanced by using a conformationally preorganized linker to connect the hydrazide units.
View Article and Find Full Text PDFInorg Chem
September 2025
College of Chemistry and Chemical Engineering, Qingdao University, Shandong 266071, P. R. China.
By adjusting the solvents, nitrogen-containing auxiliary ligands, and transition metal salts, we successfully constructed 11 new aluminum-transition heterometallic clusters of and . They possess the same metal cores with different terminal-coordinated solvents and nitrogen-containing auxiliary ligands. Given their structural differences, we investigated the variations in the photothermal effects and aldol condensation catalytic reaction.
View Article and Find Full Text PDFJ Org Chem
September 2025
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Key Laboratory of Medicinal for Natural Resource, Ministry of Education and Yunnan Province, School of Pharmacy, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China.
Herein, we report an efficient and general one-pot multicomponent strategy, innovatively developed for the construction of δ,γ-unsaturated β-hydroxy nitrile scaffolds. Using readily available aldehydes and ketones as starting materials and TMSCFBr as a difluorocarbene precursor, the transformation proceeds via tandem Aldol condensation, a difluorocarbene electrophilic reaction, and hydrolysis. Mechanistic studies revealed that the difluorocarbene activates the oxygen atom of the α,β-unsaturated carbonyl group through electrophilic orientation, significantly enhancing the electrophilicity of the carbonyl carbon, thereby driving the reaction to proceed with high selectivity via a 1,2-addition pathway.
View Article and Find Full Text PDFBMC Chem
August 2025
Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
In this study, novel linear 3-(arylamino)naphtho[2,3-b]furan-2,4,9(3H)-trione derivatives has been synthesized via annulation reaction of 2-hydroxy-1,4-naphthoquinone with aromatic amines and glyoxylic acid monohydrate using p-TSOH as catalyst at ambient temperature for the first time. The mechanism proceeds via an initial intermolecular aldol condensation, subsequent Michael addition, and final intramolecular nucleophilic annulation. The linear or angular configurations of the products was confirmed through - C heteronuclear multiple-bond correlation (HMBC) analysis.
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