Fixing Flexible Arms of Core-Shared Ligands to Enhance the Stability of Metal–Organic Frameworks

2019 ◽  
Vol 58 (23) ◽  
pp. 15909-15916 ◽  
Author(s):  
Chen Dong ◽  
Jinquan Bai ◽  
Xiu-Liang Lv ◽  
Wei Wu ◽  
Jie Lv ◽  
...  
2010 ◽  
Vol 46 (33) ◽  
pp. 6120 ◽  
Author(s):  
Tianjiao Wu ◽  
Lingjuan Shen ◽  
Matthew Luebbers ◽  
Chunhua Hu ◽  
Qingmei Chen ◽  
...  

2016 ◽  
Vol 52 (55) ◽  
pp. 8501-8513 ◽  
Author(s):  
Na Li ◽  
Jian Xu ◽  
Rui Feng ◽  
Tong-Liang Hu ◽  
Xian-He Bu

Stability of MOFs is a crucial issue for their practical applications, which might be improved by varying their chemical composition and/or structurally tuning them. Several strategies for enhancing the stability of MOFs were provided.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Mathieu Bosch ◽  
Muwei Zhang ◽  
Hong-Cai Zhou

Metal-organic frameworks (MOFs) are a new category of advanced porous materials undergoing study by many researchers for their vast variety of both novel structures and potentially useful properties arising from them. Their high porosities, tunable structures, and convenient process of introducing both customizable functional groups and unsaturated metal centers have afforded excellent gas sorption and separation ability, catalytic activity, luminescent properties, and more. However, the robustness and reactivity of a given framework are largely dependent on its metal-ligand interactions, where the metal-containing clusters are often vulnerable to ligand substitution by water or other nucleophiles, meaning that the frameworks may collapse upon exposure even to moist air. Other frameworks may collapse upon thermal or vacuum treatment or simply over time. This instability limits the practical uses of many MOFs. In order to further enhance the stability of the framework, many different approaches, such as the utilization of high-valence metal ions or nitrogen-donor ligands, were recently investigated. This review details the efforts of both our research group and others to synthesize MOFs possessing drastically increased chemical and thermal stability, in addition to exemplary performance for catalysis, gas sorption, and separation.


2018 ◽  
Vol 9 (4) ◽  
pp. 950-955 ◽  
Author(s):  
Rui Feng ◽  
Yan-Yuan Jia ◽  
Zhao-Yang Li ◽  
Ze Chang ◽  
Xian-He Bu

Guided by the insertion of coordination sites within ligands, an interpenetrated metal–organic framework (MOFs) NKU-112 and a self-penetrated framework NKU-113 were obtained. The enhanced stability and porosity of NKU-113 prove the efficiency of the method for the structure and properties modulation of penetrated MOFs.


2018 ◽  
pp. 1-28 ◽  
Author(s):  
Georges Mouchaham ◽  
Sujing Wang ◽  
Christian Serre

2019 ◽  
Vol 141 (26) ◽  
pp. 10283-10293 ◽  
Author(s):  
Xiu-Liang Lv ◽  
Shuai Yuan ◽  
Lin-Hua Xie ◽  
Hannah F. Darke ◽  
Ya Chen ◽  
...  

2015 ◽  
Vol 119 (29) ◽  
pp. 8992-8999 ◽  
Author(s):  
Harsha V. R. Annapureddy ◽  
Satish K. Nune ◽  
Radha Kishan Motkuri ◽  
B. Peter McGrail ◽  
Liem X. Dang

2021 ◽  
Author(s):  
Daniele Cartagenova ◽  
Fabio A. Peixoto Esteves ◽  
Nathan T. Fischer ◽  
Jeroen A. van Bokhoven ◽  
Marco Ranocchiari

UiO-66 is one of the most chemically stable Metal-organic frameworks (MOFs) available. However, little is known about its stability in organic solvents. In this study, we synthesized a highly defective UiO-66 (HD-UiO-66) and explored how its textural properties change when exposed to weak and strong acids, both organic and inorganic in nature, and dissolved in different solvents, water, dichloromethane (DCM), and tetrahydrofuran (THF). Exposing defective UiO-66 to weak acids and bases, such as acetic acid and triethylamine, maintains its crystalline structure and porosity, irrespective of the solvent. Sulphuric acid decomposes HD-UiO-66 in organic solvents but not in water, trifluoroacetic acid decomposes the framework only in DCM. Tetramethylguanidine decomposes HD-UiO-66 in organic solvents but mantains some of the MOFs porosity and crystalline structure in water, whereas potassium carbonate damages the MOF to a greater extent in water than in organic solvents. Our results show that the acid/base properties of the solvent modulate the strength of acids and bases and its polarity determines the extent of their solvation, thus playing a crucial role in altering the MOF’s textural properties. This systematic investigation highlights the central role played by the solvent in tuning the stability of MOFs, which is relevant for liquid-phase applications in acidic and basic environments, such as catalysis and adsorption.


2021 ◽  
Author(s):  
Daniele Cartagenova ◽  
Fabio A. Peixoto Esteves ◽  
Nathan T. Fischer ◽  
Jeroen A. van Bokhoven ◽  
Marco Ranocchiari

UiO-66 is one of the most chemically stable Metal-organic frameworks (MOFs) available. However, little is known about its stability in organic solvents. In this study, we synthesized a highly defective UiO-66 (HD-UiO-66) and explored how its textural properties change when exposed to weak and strong acids, both organic and inorganic in nature, and dissolved in different solvents, water, dichloromethane (DCM), and tetrahydrofuran (THF). Exposing defective UiO-66 to weak acids and bases, such as acetic acid and triethylamine, maintains its crystalline structure and porosity, irrespective of the solvent. Sulphuric acid decomposes HD-UiO-66 in organic solvents but not in water, trifluoroacetic acid decomposes the framework only in DCM. Tetramethylguanidine decomposes HD-UiO-66 in organic solvents but mantains some of the MOFs porosity and crystalline structure in water, whereas potassium carbonate damages the MOF to a greater extent in water than in organic solvents. Our results show that the acid/base properties of the solvent modulate the strength of acids and bases and its polarity determines the extent of their solvation, thus playing a crucial role in altering the MOF’s textural properties. This systematic investigation highlights the central role played by the solvent in tuning the stability of MOFs, which is relevant for liquid-phase applications in acidic and basic environments, such as catalysis and adsorption.


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