Modulator-Directed Counterintuitive Catenation Control for Crafting Highly Porous and Robust Metal–Organic Frameworks with Record High SO<sub>2</sub> Uptake Capacity

Sulfur dioxide (SO<sub>2</sub>) is an important industrial feedstock that can be directly utilized or catalytically transformed to value-added chemicals such as sulfuric acid. The development of regenerable porous sorbents for the highly efficient storage and energy-minimal release of toxic SO<sub>2</sub> operating under ambient conditions has attracted growing interest. Herein, we report the topology-guided construction of highly porous <b>acs</b>-type metal-organic frameworks (MOFs) through a counterintuitive modulator-directed catenation control approach. In contrast to the conventional modulator facilitated coordination competition that favors the thermodynamic catenated phase, we show that the elevation of modulator concentration can promote the formation of the noncatenated phase probably through a sublattice dissolution pathway. The assembly of a custom-designed trigonal prismatic triptycene-quinoxaline linker and trinuclear Fe<sub>3</sub>O cluster affords either the threefold catenated SJTU-219 or noncatenated SJTU-220 with desired <b>acs</b> net. Impressively, the synthetic approach is applicable to various metal ions, including Al<sup>3+</sup>, V<sup>3+</sup>, and even Ti<sup>4+</sup>. The noncatenated SJTU-220 exhibits an extraordinary SO<sub>2</sub> sorption capacity of 29.6 mmol g<sup>-1</sup> at 298 K and 1 bar, surpassing all reported solid sorbents. The uptake capacity can be further raised to 35.6 mmol g<sup>-1</sup> via the replacement of Fe<sup>3+</sup> with kinetically more inert Cr<sup>3+</sup>, resulting in a staggering ∼329-fold volume reduction compared with free ideal SO<sub>2</sub> gas. Computational simulations suggest that unique Fe<sup>3+</sup>···S(SO<sub>2</sub>) interactions dominate the SO<sub>2</sub> seeding process, facilitating the efficient packing of SO<sub>2</sub> molecules in the large channels. Besides, the exceptionally low uptake at the low pressure region implies global weak framework-SO<sub>2</sub> interactions, which offer great potential for practically implementing an "easy-on/easy-off" SO<sub>2</sub> delivery system.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-11-07
DOI
https://doi.org/10.1021/jacs.4c10723
Citations
21
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
3.33

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article

Modulator-Directed Counterintuitive Catenation Control for Crafting Highly Porous and Robust Metal–Organic Frameworks with Record High SO2 Uptake Capacity

Wei Gong, Yong Cui, Jinqiao Dong, Xiaoliang Wang et al.
21 citations
Journal of the American Chemical Society
Metal-Organic Frameworks: Synthesis and Applications
3.33
article

Modulator-Directed Counterintuitive Catenation Control for Crafting Highly Porous and Robust Metal–Organic Frameworks with Record High SO2 Uptake Capacity

Wei Gong, Yong Cui, Jinqiao Dong, Xiaoliang Wang, Pengfu Gao, Yi Xie, Xing Han, Xianhui Tang, Kun Wang, Zhijie Chen, Yifei Gao, Jingjing Zhang
article en
21 citations

Abstract

Sulfur dioxide (SO<sub>2</sub>) is an important industrial feedstock that can be directly utilized or catalytically transformed to value-added chemicals such as sulfuric acid. The development of regenerable porous sorbents for the highly efficient storage and energy-minimal release of toxic SO<sub>2</sub> operating under ambient conditions has attracted growing interest. Herein, we report the topology-guided construction of highly porous <b>acs</b>-type metal-organic frameworks (MOFs) through a counterintuitive modulator-directed catenation control approach. In contrast to the conventional modulator facilitated coordination competition that favors the thermodynamic catenated phase, we show that the elevation of modulator concentration can promote the formation of the noncatenated phase probably through a sublattice dissolution pathway. The assembly of a custom-designed trigonal prismatic triptycene-quinoxaline linker and trinuclear Fe<sub>3</sub>O cluster affords either the threefold catenated SJTU-219 or noncatenated SJTU-220 with desired <b>acs</b> net. Impressively, the synthetic approach is applicable to various metal ions, including Al<sup>3+</sup>, V<sup>3+</sup>, and even Ti<sup>4+</sup>. The noncatenated SJTU-220 exhibits an extraordinary SO<sub>2</sub> sorption capacity of 29.6 mmol g<sup>-1</sup> at 298 K and 1 bar, surpassing all reported solid sorbents. The uptake capacity can be further raised to 35.6 mmol g<sup>-1</sup> via the replacement of Fe<sup>3+</sup> with kinetically more inert Cr<sup>3+</sup>, resulting in a staggering ∼329-fold volume reduction compared with free ideal SO<sub>2</sub> gas. Computational simulations suggest that unique Fe<sup>3+</sup>···S(SO<sub>2</sub>) interactions dominate the SO<sub>2</sub> seeding process, facilitating the efficient packing of SO<sub>2</sub> molecules in the large channels. Besides, the exceptionally low uptake at the low pressure region implies global weak framework-SO<sub>2</sub> interactions, which offer great potential for practically implementing an "easy-on/easy-off" SO<sub>2</sub> delivery system.

Journal of the American Chemical SocietyVol. 146(46)
Northwestern University (US), Shanghai Jiao Tong University (CN), Zhejiang University (CN)
Shanghai Key Basic Research Program, National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, Shanghai Municipal Human Resources and Social Security Bureau, Science, Technology and Innovation Commission of Shenzhen Municipality, National Key Research and Development Program of China
Openalex Percentile: Top 7%
Metal-Organic Frameworks: Synthesis and Applications
3.33
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