New chemical compositions and structures for medium- and high-entropy oxides (HEOs) currently represent a promising new avenue in materials research for a wide range of applications including catalysis, energy storage, and ceramics. To speed up further development, synthesis methods for multicationic oxides are needed for controlling features like morphology, porosity, and chemical compositions. In this work, mesoporous spinel oxide spheres with five cations are synthesized using solvothermal synthesis techniques. The targeted chemistry included Co, Al, Fe, and Cr as the first four cations, where the fifth cation was varied by increasing cation radii (Ga, In, Yb, Ho, or Ce). After calcination, all as-synthesized precursors led to mesoporous oxide spheres with spinel oxide structures. In order to demonstrate an example of applicability for targeting different M cations, the sample containing Co, Al, Fe, Cr, and In was tested in a model reaction of thermocatalytic CO hydrogenation and is shown to be active with a preference to methanol formation (58 % selectivity, 7.8 % conversion at 300 °C). The synthesis of multicationic mesoporous spheres appears to be quite flexible in terms of possible M cations compositions and is a potential material to combine targeted chemistry for applications like catalysis.
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http://dx.doi.org/10.1002/cplu.202400691 | DOI Listing |
Org Lett
January 2025
China Guangxi Key Laboratory of Pharmaceutical Precision Detection and Screening, Guangxi Key Laboratory of Bioactive Molecules Research and Evaluation, and Key Laboratory of Micro-Nanoscale Bioanalysis and Drug Screening of Guangxi Education Department, Pharmaceutical College, Guangxi Medical University, Nanning 530021, China.
Herein, a one-pot domino catalyzed three-component process is described, which is initiated by a palladium/zinc cooperatively catalyzed cycloaddition between trimethylenemethane (TMM) and unactivated alkyl/aryl imines, followed by one-pot isomerization and Zn(OTf)-catalyzed DDQ oxidation, furnishing valuable substituted pyrroles. We disclose that the palladium/zinc cooperative catalysis affords a dual-Zn(OTf)-stabilized azapalladacycle, wherein the Pd-N bond is polarized by Zn(OTf), facilitating a unique outer-sphere allylic amination. Moreover, subsequent DDQ dehydrogenation can be feasibly promoted by zinc catalysis.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry and Nuclear Science & Engineering Center, Colorado School of Mines, Golden, Colorado 80401, United States.
The and isomers of [Sm(dicyclohexano-18-crown-6)(HO)]I exhibiting water molecules bound to the Sm ion have been isolated and characterized. Sm possesses an electrochemical potential sufficient for water reduction, and thus these complexes add to the recent body of evidence that the oxidation of Sm by water can operate by a mechanism that is not straightforward. These complexes are obtained by the direct addition of stoichiometric amounts of water to solutions of the respective Sm(dicyclohexano-18-crown-6)I isomers under an inert atmosphere.
View Article and Find Full Text PDFMolecules
December 2024
Department of Physical Chemistry, Gdańsk University of Technology, Narutowicza 11/12, 80-233 Gdańsk, Poland.
This study provides a comprehensive analysis of the interactions between dimethyl sulfoxide (DMSO) and two small peptides, diglycine and -acetyl-glycine-methylamide (NAGMA), in aqueous solutions using FTIR spectroscopy and density functional theory (DFT) calculations. ATR-FTIR spectroscopy and DFT results revealed that DMSO does not form direct bonds with the peptides, suggesting that DMSO indirectly influences both peptides by modifying the surrounding water molecules. The analysis of HDO spectra allowed for the isolation of the contribution of water molecules that were simultaneously altered by the peptide and DMSO, and it also explained the changes in the hydration shells of the peptides in the presence of DMSO.
View Article and Find Full Text PDFFEMS Microbiol Ecol
January 2025
Center for Pan-third Pole Environment, Lanzhou University, Lanzhou, China.
In polar and alpine regions, global warming and landform changes are draining lakes, transforming them into permafrost with altered microbial communities and element cycling. In this study, we investigated bacterial and archaeal (prokaryotic) community changes in the newly exposed sediment of Zonag Lake (Tibetan Plateau), focusing on prokaryotic diversity, community structure, and genes involved in carbon fixation and nitrogen cycling across lateral (up to 800 m) and vertical (up to 80 cm) horizons. The results showed that prokaryotic richness decreased across the lateral horizons, coinciding with reductions in carbon concentrations.
View Article and Find Full Text PDFChemosphere
January 2025
Departamento de Química, Universidade Federal do Paraná, 81531-980, Curitiba, PR, Brazil.
Soil is regarded as a natural repository for strongly adsorbed pollutants since glyphosate (GLY) is preferentially adsorbed by the inorganic fraction of the soil, which may greatly limits its leaching. In this way, understanding how clay mineralogy influences the sorption and transport processes of glyphosate in soils with different mineralogical characteristics is highly relevant. In this work, two clay mineralogy contrasting soils were used to evaluate GLY retention: a Oxisol (OX) with high levels of iron oxides (amorphous and crystalline) and a Inceptisol (IN) with a predominance of kaolinite.
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