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用于水吸附的单晶多模块铬(III)金属有机框架的合成

Synthesis of Single-Crystalline Multi-Module Chromium(III) Metal-Organic Frameworks for Water Adsorption.

作者信息

Huang Yexin, Zhang Zhenghan, Tao Yongcheng, Zhu Kai, Huang Xinyi, Yang Yijun, Huang Hongliang, Li Jian, Yang Huajun

机构信息

Jiangsu Key Laboratory of Biomedical Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.

State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.

出版信息

JACS Au. 2025 May 30;5(6):2533-2541. doi: 10.1021/jacsau.5c00148. eCollection 2025 Jun 23.

DOI:10.1021/jacsau.5c00148
PMID:40575323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12188484/
Abstract

The robust Cr-(III) metal-organic frameworks (MOFs) have attracted considerable interest in water adsorptions. However, the synthesis of highly crystalline Cr-MOFs is complicated by the kinetically inert nature of Cr-(III). The main method for the preparation of Cr-MOFs now is postsynthetic metathesis, which is all consuming. Here, we report the synthesis of a series of multi-module, single-crystalline Cr-MOFs at the micro scale (up to 6 μm). A dual-modulator (HF-pyridine) strategy is developed to modulate the multiple competitive coordination bonding in dual-ligand-based Cr-MOFs, with the secondary modulator of pyridine having the functional group of the secondary module of tripyridyl ligands, which thus acts as an additional inhibitor to nucleation. The high crystallinity has enabled the structure determination of a novel Cr-MOF (Cr-bpdc-tph) at atomic resolution by the continuous rotation electron diffraction (cRED) technique. Cr-bpdc-tph integrates both high porosity with a BET surface area up to 3191 m/g and exceptional chemical resistance in extreme acidic and basic solutions (pH < 0 and pH > 14). The water adsorption results show that Cr-bpdc-tph has achieved an effective working efficiency of 76% within the relative humidity range of 45-65%.

摘要

坚固的Cr(III)金属有机框架(MOF)在水吸附方面引起了广泛关注。然而,Cr(III)的动力学惰性使得高结晶度Cr-MOF的合成变得复杂。目前制备Cr-MOF的主要方法是后合成复分解法,这种方法消耗量大。在此,我们报告了一系列多模块、单晶Cr-MOF在微观尺度(最大6μm)上的合成。开发了一种双调节剂(HF-吡啶)策略来调节基于双配体的Cr-MOF中的多重竞争配位键,吡啶作为二级调节剂,具有三联吡啶配体二级模块的官能团,因此可作为成核的额外抑制剂。高结晶度使得通过连续旋转电子衍射(cRED)技术在原子分辨率下确定了一种新型Cr-MOF(Cr-bpdc-tph)的结构。Cr-bpdc-tph兼具高达3191 m²/g的BET表面积的高孔隙率和在极端酸性和碱性溶液(pH < 0和pH > 14)中的优异耐化学性。水吸附结果表明,Cr-bpdc-tph在45 - 65%的相对湿度范围内实现了76%的有效工作效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/c34ee400f94d/au5c00148_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/7757146a737f/au5c00148_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/60e2c55e47cf/au5c00148_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/73ea4d5e53af/au5c00148_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/226259df50c6/au5c00148_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/c34ee400f94d/au5c00148_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/7757146a737f/au5c00148_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/60e2c55e47cf/au5c00148_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/73ea4d5e53af/au5c00148_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/226259df50c6/au5c00148_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e9/12188484/c34ee400f94d/au5c00148_0005.jpg

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Programmable Water Sorption through Linker Installation into a Zirconium Metal-Organic Framework.
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Chiral Reticular Chemistry: A Tailored Approach Crafting Highly Porous and Hydrolytically Robust Metal-Organic Frameworks for Intelligent Humidity Control.手性网状化学:一种定制方法,用于构建高度多孔且耐水解的金属有机框架以实现智能湿度控制。
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