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Hexacoordinate Ti-Anchored Single-Atom Pd Catalyst for High-Efficiency Cyclohexanone Ammoximation with H and O.

Journal of the American Chemical Society 2026 Catalysts for Methane Reforming
OpenAlex 토픽 · Catalysts for Methane Reforming Catalysis for Biomass Conversion Carbon dioxide utilization in catalysis

Zhai C, Dong Z, Ma Y, Gong X, Yang T, Wan Z, Gao M, Lin H, Liu Y, Jin S, Wang R, Ren G, Wu P, Ma Y, Xu H

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Integrating Pd or its alloys with titanosilicate zeolites enables the production of cyclohexanone oxime through the ammoximation reaction of cyclohexanone with H and O instead of relying on HO produce

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BibTeX ↓ RIS ↓
APA Chengwei Zhai, Zhuoya Dong, et al. (2026). Hexacoordinate Ti-Anchored Single-Atom Pd Catalyst for High-Efficiency Cyclohexanone Ammoximation with H and O.. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.6c01171
MLA Chengwei Zhai, et al.. "Hexacoordinate Ti-Anchored Single-Atom Pd Catalyst for High-Efficiency Cyclohexanone Ammoximation with H and O.." Journal of the American Chemical Society, 2026.
PMID 42008295

Abstract

Integrating Pd or its alloys with titanosilicate zeolites enables the production of cyclohexanone oxime through the ammoximation reaction of cyclohexanone with H and O instead of relying on HO produced in advance. To address the inefficient utilization of precious metals and the suboptimal Ti activity in existing composite catalysts, we innovatively employed Ti-MWW zeolite as a support to develop a brand-new bifunctional catalyst Pd@Ti-MWW-PI through a one-step synthesis, constructing a unique active site where piperidine-modified Pd single atoms are anchored on the hexacoordinated framework-Ti via the Pd-O-Ti bond. This catalyst with an ultralow Pd loading of 0.02 wt % attains a record cyclohexanone oxime formation rate of 13000 mol mol h and demonstrates exceptional stability in continuous fixed-bed operation, sustaining cyclohexanone oxime selectivity greater than 99% for more than 2500 h. Notably, this work, utilizing water as the solvent, marks a significant stride toward environmentally sustainable green chemistry and bolsters the practical feasibility of H/O-mediated ammoximation.

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