Lone-pair-electron-governed gas-recognizable flexibility in a stable MOF for boosting C3H6/C3H8 separation via aqueous scalable synthesis

The separation of propylene from propane constitutes one of the most energy-demanding processes in the petrochemical industry due to their similar molecular dimensions and physicochemical properties. Flexible MOFs, which undergo selective guest-induced structural transformations, offer an alternative mechanism to amplify subtle molecular differences into distinct adsorption behaviors. Nevertheless, the precise molecular-level modulation of framework flexibility to elicit a selective response to one specific gas over another remains a great challenge. This study confronts this challenge through the rational structural evolution of a hydrolytically stable, pillar-layered Cu-MOF, NJU-Bai5. Our strategy involves the strategic engineering of the pillar ligand, specifically replacing pyridyl with imidazolyl groups. This modification introduces accessible nitrogen lone-pair-electrons, which function as molecular anchors capable of forming selective interactions with hydrogen-bonding donors possessing higher acidity. These interactions, in turn, drive a gas-recognizable flexibility of the framework. The resulting material, NJU-Bai5-bib, exhibits a well-defined, selective gate-opening transition triggered preferentially by C3H6 at low pressures. This specific response enables the framework to achieve highly selective propylene/propane separation under ambient conditions. Furthermore, by inheriting exceptional hydrolytic stability from its progenitor and featuring a scalable, aqueous synthesis, NJU-Bai5-bib demonstrates not only excellence in guest-specific recognition but also considerable potential for practical, energy-efficient propylene purification. The introduction of nitrogen lone-pair-electrons in a hydrolytically stable MOF NJUBai5-bib enabling C3H6-recognizable gate-opening towards efficient C3H6/C3H8 separation and the scalable aqueous synthesis of it for environmentally friendly application.

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Publication Details

Journal
Nature Communications
Published
2026-07-22
DOI
https://doi.org/10.1038/s41467-026-75928-3
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
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article

Lone-pair-electron-governed gas-recognizable flexibility in a stable MOF for boosting C3H6/C3H8 separation via aqueous scalable synthesis

Junfeng Bai, Zhiyong Lu, Lilei Zhang, Banghao Wei et al.
Nature Communications
Metal-Organic Frameworks: Synthesis and Applications
article

Lone-pair-electron-governed gas-recognizable flexibility in a stable MOF for boosting C3H6/C3H8 separation via aqueous scalable synthesis

Junfeng Bai, Zhiyong Lu, Lilei Zhang, Banghao Wei, Y Jiang, Yuhang Liu, Bufeng Wang
article en

Abstract

The separation of propylene from propane constitutes one of the most energy-demanding processes in the petrochemical industry due to their similar molecular dimensions and physicochemical properties. Flexible MOFs, which undergo selective guest-induced structural transformations, offer an alternative mechanism to amplify subtle molecular differences into distinct adsorption behaviors. Nevertheless, the precise molecular-level modulation of framework flexibility to elicit a selective response to one specific gas over another remains a great challenge. This study confronts this challenge through the rational structural evolution of a hydrolytically stable, pillar-layered Cu-MOF, NJU-Bai5. Our strategy involves the strategic engineering of the pillar ligand, specifically replacing pyridyl with imidazolyl groups. This modification introduces accessible nitrogen lone-pair-electrons, which function as molecular anchors capable of forming selective interactions with hydrogen-bonding donors possessing higher acidity. These interactions, in turn, drive a gas-recognizable flexibility of the framework. The resulting material, NJU-Bai5-bib, exhibits a well-defined, selective gate-opening transition triggered preferentially by C3H6 at low pressures. This specific response enables the framework to achieve highly selective propylene/propane separation under ambient conditions. Furthermore, by inheriting exceptional hydrolytic stability from its progenitor and featuring a scalable, aqueous synthesis, NJU-Bai5-bib demonstrates not only excellence in guest-specific recognition but also considerable potential for practical, energy-efficient propylene purification. The introduction of nitrogen lone-pair-electrons in a hydrolytically stable MOF NJUBai5-bib enabling C3H6-recognizable gate-opening towards efficient C3H6/C3H8 separation and the scalable aqueous synthesis of it for environmentally friendly application.

Nature Communications
Nanjing Tech University (CN), Luoyang Normal University (CN)
Responsible consumption and production
Openalex Percentile: Top 19%
Metal-Organic Frameworks: Synthesis and Applications
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