Constructing multiple active sites in iron oxide catalysts for improving carbonylation reactions

Surface engineering is a promising strategy to improve the catalytic activities of heterogeneous catalysts. Nevertheless, few studies have been devoted to investigate the catalytic behavior differences of the multiple metal active sites triggered by the surface imperfections on catalysis. Herein, ox...

Full description

Saved in:
Bibliographic Details
Published in:Nature communications Vol. 14; no. 1; p. 4973
Main Authors: Liu, Shujuan, Li, Teng, Shi, Feng, Ma, Haiying, Wang, Bin, Dai, Xingchao, Cui, Xinjiang
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 17-08-2023
Nature Publishing Group
Nature Portfolio
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Surface engineering is a promising strategy to improve the catalytic activities of heterogeneous catalysts. Nevertheless, few studies have been devoted to investigate the catalytic behavior differences of the multiple metal active sites triggered by the surface imperfections on catalysis. Herein, oxygen vacancies induced Fe 2 O 3 catalyst are demonstrated with different Fe sites around one oxygen vacancy and exhibited significant catalytic performance for the carbonylation of various aryl halides and amines/alcohols with CO. The developed catalytic system displays excellent activity, selectivity, and reusability for the synthesis of carbonylated chemicals, including drugs and chiral molecules, via aminocarbonylation and alkoxycarbonylation. Combined characterizations disclose the formation of oxygen vacancies. Control experiments and density functional theory calculations demonstrate the selective combination of the three Fe sites is vital to improve the catalytic performance by catalyzing the elemental steps of PhI activation, CO insertion and C-N/C-O coupling respectively, endowing combinatorial sites catalyst for multistep reactions. Surface engineering of Fe sites was used to improve the carbonylation reaction of aryl halides and amines/alcohols with CO. The elementary steps of phenyl iodide activation, CO insertion and C-N/C-O coupling were catalyzed respectively, leading to improved catalytic activity.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-40640-z