scholarly journals Post-synthetic ligand exchange in zirconium-based metal-organic frameworks: beware of the defects!

Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

<p>Post-synthetic ligand exchange is a valuable synthetic tool for functionalisation of zirconium-based metal-organic frameworks. It is generally assumed that the exchange involves organic linkers, however these materials are known to contain large amounts of defects, which are likely to play a role during the exchange process. This can eventually lead to unexpected effects on the physical-chemical properties of the material. Post-synthetic ligand exchange in the prototypical zirconium-based metal-organic framework UiO-66 was investigated by <i>in situ</i> solution nuclear magnetic resonance. Samples of UiO-66 prepared either with or without modulators (formic acid or benzoic acid) and having different degrees of defectivity were exchanged using solutions of 2,5-pyridinedicarboxylic acid at different temperatures. Linker exchange only occurred in a defect-free UiO-66, whereas monocarboxylates grafted at defective sites were found to be preferentially exchanged with respect to terephthalic acid over the whole range of conditions investigated. A 1:1 exchange ratio between 2,5-pyridinedicarboxylic acid and modulator was observed, providing evidence that the defects had missing-cluster nature. These findings were corroborated by <i>ex situ</i> characterisation of exchanged samples.</p>

2018 ◽  
Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

<p>Post-synthetic ligand exchange is a valuable synthetic tool for functionalisation of zirconium-based metal-organic frameworks. It is generally assumed that the exchange involves organic linkers, however these materials are known to contain large amounts of defects, which are likely to play a role during the exchange process. This can eventually lead to unexpected effects on the physical-chemical properties of the material. Post-synthetic ligand exchange in the prototypical zirconium-based metal-organic framework UiO-66 was investigated by <i>in situ</i> solution nuclear magnetic resonance. Samples of UiO-66 prepared either with or without modulators (formic acid or benzoic acid) and having different degrees of defectivity were exchanged using solutions of 2,5-pyridinedicarboxylic acid at different temperatures. Linker exchange only occurred in a defect-free UiO-66, whereas monocarboxylates grafted at defective sites were found to be preferentially exchanged with respect to terephthalic acid over the whole range of conditions investigated. A 1:1 exchange ratio between 2,5-pyridinedicarboxylic acid and modulator was observed, providing evidence that the defects had missing-cluster nature. These findings were corroborated by <i>ex situ</i> characterisation of exchanged samples.</p>


2018 ◽  
Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

<p>Post-synthetic ligand exchange in the prototypical zirconium-based metal-organic framework UiO-66 was investigated by in situ solution <sup>1</sup>H nuclear magnetic resonance. Samples of UiO-66 having different degrees of defectivity were exchanged using solutions of several terephthalic acid analogues in a range of conditions. Linker exchange only occurred in defect-free UiO-66, whereas monocarboxylates grafted at defective sites were found to be preferentially exchanged with respect to terephthalic acid over the whole range of conditions investigated. A 1:1 exchange ratio between the terephthalic acid analogue and modulator was observed, providing evidence that the defects had missing-cluster nature. Ex situ characterisation of the MOF powders after exchange corroborated these findings and evidenced that the physical-chemical properties of the MOF depend on whether the functionalisation occurs at defective sites or on the framework. N<sub>2</sub> sorption analysis showed that, upon exchange, defective samples underwent significant decrease of surface area and disappearance of large pores, associated with the presence of missing-cluster defects in the starting material. CO<sub>2 </sub>sorption studies displayed the different impact of pure defect functionalisation and pure framework functionalisation on isosteric heat of adsorption and CO<sub>2</sub>/N<sub>2</sub> selectivity.</p>


2018 ◽  
Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

<p>Post-synthetic ligand exchange in the prototypical zirconium-based metal-organic framework UiO-66 was investigated by in situ solution <sup>1</sup>H nuclear magnetic resonance. Samples of UiO-66 having different degrees of defectivity were exchanged using solutions of several terephthalic acid analogues in a range of conditions. Linker exchange only occurred in defect-free UiO-66, whereas monocarboxylates grafted at defective sites were found to be preferentially exchanged with respect to terephthalic acid over the whole range of conditions investigated. A 1:1 exchange ratio between the terephthalic acid analogue and modulator was observed, providing evidence that the defects had missing-cluster nature. Ex situ characterisation of the MOF powders after exchange corroborated these findings and evidenced that the physical-chemical properties of the MOF depend on whether the functionalisation occurs at defective sites or on the framework. N<sub>2</sub> sorption analysis showed that, upon exchange, defective samples underwent significant decrease of surface area and disappearance of large pores, associated with the presence of missing-cluster defects in the starting material. CO<sub>2 </sub>sorption studies displayed the different impact of pure defect functionalisation and pure framework functionalisation on isosteric heat of adsorption and CO<sub>2</sub>/N<sub>2</sub> selectivity.</p>


2018 ◽  
Vol 130 (36) ◽  
pp. 11880-11884 ◽  
Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

2020 ◽  
Author(s):  
Katrina Penticoff ◽  
Jessica C. Moreton ◽  
Jin Low ◽  
Zisheng Ye ◽  
Seth Cohen ◽  
...  

2020 ◽  
Author(s):  
Katrina Penticoff ◽  
Jessica C. Moreton ◽  
Jin Low ◽  
Zisheng Ye ◽  
Seth Cohen ◽  
...  

Rare Metals ◽  
2019 ◽  
Vol 38 (5) ◽  
pp. 413-419 ◽  
Author(s):  
Xiao-Hui Chen ◽  
Qin Wei ◽  
Jin-Dui Hong ◽  
Rong Xu ◽  
Tian-Hua Zhou

2020 ◽  
Author(s):  
Katrina Penticoff ◽  
Jessica C. Moreton ◽  
Jin Low ◽  
Zisheng Ye ◽  
Seth Cohen ◽  
...  

2018 ◽  
Vol 57 (36) ◽  
pp. 11706-11710 ◽  
Author(s):  
Marco Taddei ◽  
Russell J. Wakeham ◽  
Athanasios Koutsianos ◽  
Enrico Andreoli ◽  
Andrew R. Barron

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