Excision in Reduced Dimensionality: Synthesis of 1D Covalent Organic Framework via Clip‐off Chemistry

T Tongyan Li (Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China) A Ai‐Juan Li (MOE Key Laboratory of Cluster Science School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing China) Z Zichen Cai (Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China) S Shuyu Dong (Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China) T Tongxuan Li (Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China) J Jing Li N Naifang Liu (Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China) J Jianzhuang Jiang (Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry and Chemical Engineering, School of Chemistry and Biological Engineering)

Abstract

ABSTRACT Synthesizing 1D COFs with a tailored chain stacking model is a significant challenge. Here, we introduce a novel preparation approach of 1D COFs involving selective excision from 2D matrix via clip‐off chemistry. We carefully designed a 2D sql framework incorporating strategically cleavable olefinic linkers, enabling transformation of X‐shaped tetratopic linkers into V‐shaped ditopic counterparts through ozonolysis. The resulting 1D COF, featuring carboxyl group, was then functionalized with Anderson‐type POMs via Schiff base reactions. This POM‐COF composite demonstrated enhanced photocatalytic aldehyde oxidation, benefiting from synergistic effects to achieve efficient and selective conversion of aldehydes to carboxylic acids. Our work offers valuable insights for the custom synthesis of 1D COFs with predefined chain arrangements and functional orientations.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

T

Tongyan Li

Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China

A

Ai‐Juan Li

MOE Key Laboratory of Cluster Science School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing China

Z

Zichen Cai

Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China

S

Shuyu Dong

Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China

T

Tongxuan Li

Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China

J

Jing Li

N

Naifang Liu

Beijing Key Laboratory For Science and Application of Functional Molecular and Crystalline Materials School of Chemistry and Biological Engineering University of Science and Technology Beijing Beijing China

J

Jianzhuang Jiang

Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry and Chemical Engineering, School of Chemistry and Biological Engineering