Highly Active, Ultra-Low Loading Single-Atom Iron Catalysts for Catalytic Transfer Hydrogenation

Author:

An Zhidong1,Yang Piaoping2,Duan Delong3,Li Jiang1,Wan Tong4,Kong Yue4,Caratzoulas Stavros2,Xiang Shuting5ORCID,Liu Jiaxing4,Huang Lei1,Frenkel Anatoly5ORCID,Jiang Yuan-Ye6,Long Ran3ORCID,Li Zhenxing7ORCID,Vlachos Dionisios2ORCID

Affiliation:

1. China University of Petroleum-Beijing, 18 Fuxue Road, Changping, Beijing

2. University of Delaware

3. University of Science and Technology of China

4. China University of Petroleum-Beijing

5. Stony Brook University

6. Qufu Normal University

7. China University of Petroleum, Beijing

Abstract

Abstract Highly effective and selective noble metal-free catalysts attract significant attention. Here, a single-atom iron catalyst is fabricated by saturated adsorption of trace iron onto zeolitic imidazolate framework-8 (ZIF-8) followed by pyrolysis. Its performance toward catalytic transfer hydrogenation of furfural is comparable to state-of-the-art catalysts and up to four orders higher than other Fe catalysts. Isotopic labeling experiments demonstrate an intermolecular hydride transfer mechanism. First principles simulations, spectroscopic calculations and experiments, and kinetic correlations reveal that the synthesis creates pyrrolic Fe(I)-plN3 as the active center whose flexibility manifested by being pulled out of the plane, enabled by defects, is crucial for collocating the reagents and allowing the chemistry to proceed. The catalyst catalyzes chemoselectively several substrates and possesses a unique trait whereby the chemistry is hindered for more acidic substrates than the hydrogen donors. This work paves the way toward noble-metal free single-atom catalysts for important chemical reactions.

Publisher

Research Square Platform LLC

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