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Identifying a superior Ptδ+ species for the hydrogen-borrowing amination of alcohol at low temperature.

Authors :
Jia, Shengchao
Tong, Tao
Liu, Xiaohui
Guo, Yong
Dong, Lin
Chen, Zupeng
Wang, Yanqin
Source :
Journal of Catalysis. Apr2024, Vol. 432, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

[Display omitted] • Ptδ+ species with high positive charge was identified as the most active sites. • An efficient catalyst, 0.38Pt/CeO 2 , was designed after studying the structure and performance relationship. • Hydrogen-borrowing amination can be carried out at only 80 °C with the yield of target product of 90 %. The chemical state of metallic site is crucial for the performance of supported catalysts. Due to the difference of metal-support interaction, the chemical states of the supported metallic species are usually various and identifying the most active site is therefore very important for the design of efficient catalysts. In this work, a superior Ptδ+ species with high positive charge is identified as the active site in the hydrogen-borrowing amination of cyclopentanol with cyclopentylamine via structure and performance relationship study over Pt/CeO 2 catalyst. It is found that the lower Pt loaded catalyst (0.74 %Pt/CeO 2) has much higher activity than that of the higher Pt loaded one (1.5 %Pt/CeO 2). In-situ CO-DRIFTs and XANES studies show that Pt in 0.74 %Pt/CeO 2 catalyst has higher positive charge, favoring the dehydrogenation of cyclopentanol to cyclopentanone, the rate-determining step in the whole reaction. Furthermore, a 0.38 %Pt/CeO 2 catalyst was prepared, which shows excellent performance at lower temperature (80 °C), the mildest reaction conditions investigated up to now. This work provides a new sight in the design of excellent catalysts for the hydrogen-borrowing amination under mild reaction conditions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219517
Volume :
432
Database :
Academic Search Index
Journal :
Journal of Catalysis
Publication Type :
Academic Journal
Accession number :
176431690
Full Text :
https://doi.org/10.1016/j.jcat.2024.115407