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Novel iron-tungsten catalysts were first developed for the selective catalytic reduction of NO by NH in diesel exhaust, achieving an excellent performance with a wide operating temperature window above 90% NO conversion from 225 or 250 to 450 °C (GHSVs of 30 000 or 50 000 h). It also exhibited a pronounced stability and relatively high NO conversion in the presence of HO, SO and CO. The introduction of W resulted in the formation of α-FeO and FeWO species obtained by HRTEM directly. The synergic effect of two species contributed to the high SCR activity, because of the increased surface acidity and electronic property. The FeWO with octahedral [FeO]/[WO] structure acted as the Brønsted acid sites to form highly active NH species. Combining DFT calculations with XPS and UV-vis results, it was found that the fine electron interaction between α-FeO and FeWO made the electron more easily transfer from W sites to Fe sites, which promoted the formation of NO. Judging by the kinetics and SCR activity studies, the FeWO with an appropriate W amount showed the strongest interaction, and thereby the lowest activation energy of 39 kJ•mol and optimal catalytic activity. These findings would be conducive to the reasonable design of NH-SCR catalysts by adjusting the fabrication.
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http://dx.doi.org/10.1021/acs.est.6b03589 | DOI Listing |
Chembiochem
September 2025
Science Center for Future Foods, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu, 214122, China.
Natural products exhibit a wide range of biological activities and are the crucial resources for drug development and compound modification. Cytochrome P450 enzymes (P450s, CYP) are a class of multifunctional and stereoselective biocatalysts that utilize heme as a cofactor and can be employed in the biosynthesis of natural products. With the development of biotechnology, P450s have been widely applied in the synthesis of natural products.
View Article and Find Full Text PDFChembiochem
September 2025
Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan, via Mangiagalli 25, 20133, Milan, Italy.
This study investigates the synthesis of aromatic nitriles using an evolved variant of OxdF1 (L318F/F306Y), an aldoxime dehydratase from Pseudomonas putida F1, engineered for improved catalytic efficiency toward benzaldehyde oxime. The double OxdF1 (L318F/F306Y) mutant effectively catalyzes the conversion of various benzaldoxime derivatives to the corresponding nitriles. Due to the enzyme's inherent instability, immobilized whole-cell systems are employed in a flow reactor to improve its stability and broaden its applicability, with the biotransformation of benzaldehyde oxime and 2,6-difluorobenzaldehyde oxime serving as case studies.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, LIFM, IGCME, GBRCE for Functional Molecular Engineering, Sun Yat-Sen University, Guangzhou, 510006, China.
Oximes serve as indispensable intermediates in synthetic chemistry, owing to their distinctive C═N─OH structure, conferring highly versatile reactivity. Synthesis of oxime via the electrochemical method has potential advantages, accompanied by the upgrading of industrialization. Herein, we propose a novel strategy by introducing nickel (Ni) mediation to obtain high-spin iron (Fe)(III) in phthalocyanine structure for synthesizing glyoxylate oxime via electrocatalytic nitric oxide (NO) coupling with keto acid.
View Article and Find Full Text PDFElectrophoresis
September 2025
School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, P. R. China.
In dairy products, Bacillus subtilis (B. subtilis) is considered a harmful spoilage bacterium. Consequently, it is imperative to establish highly sensitive and selective approaches for detecting B.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
Alternating current (AC) electrolysis offers a promising strategy for modulating redox states in metal-catalyzed reactions, yet its mechanistic basis remains poorly understood. Here, we uncover how AC frequency synchronizes with key steps in a Ni-catalyzed cross-coupling cycle to control product selectivity between C-N and C-C coupling. We show that optimal C-N selectivity arises from minimizing the exposure of a key intermediate, Ni(Ar)Br, to reducing conditions that otherwise promote off-cycle Ni species and undesired C-C homocoupling.
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