Zr Oxo Cluster for Cascade Conversion of Furfural to Alkyl Levulinates

Author:

Peng Qingpo1,Jiang Yongjun2,Xu Bei‐Bei3,Zhao Xiuge1,Dai Sheng2,Yao Ye‐Feng3,Hou Zhenshan1ORCID

Affiliation:

1. Key Laboratory for Advanced Materials Research Institute of Industrial Catalysis School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai 200237 P. R. China

2. Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center Institute of Fine Chemicals School of Chemistry & Molecular Engineering East China University of Science and Technology Shanghai 200237 P.R. China

3. Physics Department and Shanghai Key Laboratory of Magnetic Resonance School of Physics and Materials Science East China Normal University Shanghai 200062 P. R. China

Abstract

AbstractA novel dodecanuclear Zr oxo cluster [Zr6O4(OH)4 (HSCH2CH2COO)12]2 (ZrO‐SH‐10) has been constructed under the room temperature, followed by oxidation of the sulfhydryl group with H2O2 to achieve a bifunctional catalyst with Lewis acid and Brönsted acid sites. The characterization of catalysts indicated that {Zr6O4} cluster core can be stabilized with a shell of carboxylate ligands, and the resulting ZrO‐SO3H was formed as a discrete molecular catalyst, exhibiting superior activity and recyclability for the cascade conversion of furfural to alkyl levulinate by the integration of transfer hydrogenation and alcoholysis in n‐butanol. The yield of n‐butyl levulinate can achieve as high as 91 % under the optimum conditions. Meanwhile, no leaching of the active species was found, which confirmed the structure of the Zr oxo cluster was air and moisture‐stable. On the basis of the studies on the reaction kinetics and isotope tracking, the reaction mechanism was proposed accordingly.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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