Diffusion‐Selective Tandem Catalysis for Alkane Hydroisomerization

F Feng Yi S Shen Yu W Wen‐Tao Qiu (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) H He‐You Du (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) A An‐Kang Jiang (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) C Chun‐Mu Guo (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) J Jia‐Min Lyu (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) M Ming‐Hui Sun (Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) Z Zhao Deng Y Yi‐Long Wang (School of Chemistry, Chemical Engineering and Life Science Wuhan University of Technology Wuhan Hubei China) Y Yu Li J Jian Zhou L Li‐Hua Chen (State Key Laboratory of Advanced Technology For Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China) B Bao‐Lian Su (State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei P. R. China)

Abstract

ABSTRACT The molecular diffusion behaviors in catalytic systems can influence product selectivity. Such a phenomenon, analogous to shape selectivity in zeolite catalysis, can be referred to as diffusion‐selectivity. However, diffusion‐selectivity is often neglected, and its connotation has scarcely been revealed. Herein, a tandem diffusion system of n‐alkene and i‐alkene intermediates in catalytic hydroisomerization was precisely modulated for the demonstration of intermediate diffusion‐selective effects. In a series of Pt/zeolite composites, the diffusion distance of n‐alkene intermediates from Pt sites towards zeolitic acid sites was prolonged by depositing Pt nanoparticles at the external surface of zeolite, leading to a reduced surface permeability by 20%, which facilitated the dispersion of n‐alkene intermediates and mitigated side‐reactions. On the contrary, the diffusion length of i‐alkene intermediates inside zeolites decreased with reduced channel length, resulting in an enhanced intracrystal diffusion by two orders of magnitude, which avoided the long‐time residence in zeolite and thus the secondary cracking of i‐alkene intermediates. In this case, a high isomer yield of 62% can be obtained, outperforming the counterparts and those reported in the literature. The proposed diffusion‐selective catalysis can be generalized to reactant and product diffusion‐selectivity.

Article Details

Volume / Issue Vol. 65, Issue 23
Published June 01, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

F

Feng Yi

S

Shen Yu

W

Wen‐Tao Qiu

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

H

He‐You Du

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

A

An‐Kang Jiang

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

C

Chun‐Mu Guo

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

J

Jia‐Min Lyu

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

M

Ming‐Hui Sun

Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

Z

Zhao Deng

Y

Yi‐Long Wang

School of Chemistry, Chemical Engineering and Life Science Wuhan University of Technology Wuhan Hubei China

Y

Yu Li

J

Jian Zhou

L

Li‐Hua Chen

State Key Laboratory of Advanced Technology For Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei China

B

Bao‐Lian Su

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan Hubei P. R. China