TY - JOUR
T1 - Hexacoordinate Ti-Anchored Single-Atom Pd Catalyst for High-Efficiency Cyclohexanone Ammoximation with H2 and O2
AU - Zhai, Chengwei
AU - Dong, Zhuoya
AU - Ma, Yue
AU - Gong, Xianchen
AU - Yang, Teng
AU - Wan, Zhipeng
AU - Gao, Mingbin
AU - Lin, Haoyi
AU - Liu, Yinghui
AU - Jin, Shengbo
AU - Wang, Rui
AU - Ren, Guowei
AU - Wu, Peng
AU - Ma, Yanhang
AU - Xu, Hao
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/5/6
Y1 - 2026/5/6
N2 - Integrating Pd or its alloys with titanosilicate zeolites enables the production of cyclohexanone oxime through the ammoximation reaction of cyclohexanone with H2 and O2 instead of relying on H2O2 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 molPd–1 h–1 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 H2/O2-mediated ammoximation.
AB - Integrating Pd or its alloys with titanosilicate zeolites enables the production of cyclohexanone oxime through the ammoximation reaction of cyclohexanone with H2 and O2 instead of relying on H2O2 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 molPd–1 h–1 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 H2/O2-mediated ammoximation.
UR - https://www.scopus.com/pages/publications/105037902550
U2 - 10.1021/jacs.6c01171
DO - 10.1021/jacs.6c01171
M3 - 文章
C2 - 42008295
AN - SCOPUS:105037902550
SN - 0002-7863
VL - 148
SP - 17931
EP - 17942
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 17
ER -