scholarly journals Crystal‐Growth‐Dominated Fabrication of Metal–Organic Frameworks with Orderly Distributed Hierarchical Porosity

2019 ◽  
Vol 132 (6) ◽  
pp. 2478-2485
Author(s):  
Hang Li ◽  
Fanchen Meng ◽  
Suoying Zhang ◽  
Liguang Wang ◽  
Matthew Li ◽  
...  
2020 ◽  
Vol 59 (6) ◽  
pp. 2457-2464 ◽  
Author(s):  
Hang Li ◽  
Fanchen Meng ◽  
Suoying Zhang ◽  
Liguang Wang ◽  
Matthew Li ◽  
...  

2021 ◽  
Author(s):  
Fajar Inggit Pambudi ◽  
Michael William Anderson ◽  
Martin Attfield

Atomic force microscopy has been used to determine the surface crystal growth of two isostructural metal-organic frameworks, [Zn2(ndc)2(dabco)] (ndc = 1,4-naphthalene dicarboxylate, dabco = 4-diazabicyclo[2.2.2]octane) (1) and [Cu2(ndc)2(dabco)] (2) from...


CrystEngComm ◽  
2012 ◽  
Vol 14 (8) ◽  
pp. 2635 ◽  
Author(s):  
Beatriz Gil-Hernández ◽  
Jana K. Maclaren ◽  
Henning A. Höppe ◽  
Jorge Pasán ◽  
Joaquín Sanchiz ◽  
...  

2018 ◽  
Vol 9 (14) ◽  
pp. 3508-3516 ◽  
Author(s):  
Weibin Liang ◽  
Lin Li ◽  
Jingwei Hou ◽  
Nicholas D. Shepherd ◽  
Thomas D. Bennett ◽  
...  

The composite membranes with defective metal–organic frameworks (MOFs) show a significant increase in water flux, without compromising the high salt rejection.


ChemInform ◽  
2012 ◽  
Vol 43 (23) ◽  
pp. no-no
Author(s):  
Martin P. Attfield ◽  
Pablo Cubillas

2017 ◽  
Vol 354 ◽  
pp. 84-91 ◽  
Author(s):  
Somboon Chaemchuen ◽  
Zhixiong Luo ◽  
Kui Zhou ◽  
Bibimaryam Mousavi ◽  
Suphot Phatanasri ◽  
...  

2020 ◽  
Author(s):  
Stephen Shearan ◽  
Jannick Jacobsen ◽  
Ferdinando Costantino ◽  
Roberto D’Amato ◽  
Dmitri Novikov ◽  
...  

We report on the results of a thorough <i>in situ</i> synchrotron powder X-ray diffraction study of the crystallisation in aqueous medium of two recently discovered perfluorinated Ce(IV)-based metal-organic frameworks (MOFs), analogues of the already well investigated Zr(IV)-based UiO-66 and MIL-140A, namely, F4_UiO-66(Ce) and F4_MIL-140A(Ce). The two MOFs were originally obtained in pure form in similar conditions, using ammonium cerium nitrate and tetrafluoroterephthalic acid as building blocks, and small variations of the reaction parameters were found to yield mixed phases. Here, we investigate the crystallisation of these compounds <i>in situ</i> in a wide range of conditions, varying parameters such as temperature, amount of the protonation modulator nitric acid (HNO<sub>3</sub>) and amount of the coordination modulator acetic acid (AcOH). When only HNO<sub>3</sub> is present in the reaction environment, F4_MIL-140A(Ce) is obtained as a pure phase. Heating preferentially accelerates nucleation, which becomes rate determining below 57 °C, whereas the modulator influences nucleation and crystal growth to a similar extent. Upon addition of AcOH to the system, alongside HNO<sub>3</sub>, mixed-phased products, consisting of F4_MIL-140A(Ce) and F4_UiO-66(Ce), are obtained. In these conditions, F4_UiO-66(Ce) is always formed faster and no interconversion between the two phases occurs. In the case of F4_UiO-66(Ce), crystal growth is always the rate determining step. An increase in the amount of HNO<sub>3</sub> slows down both nucleation and growth rates for F4_MIL-140A(Ce), whereas nucleation is mainly affected for F4_UiO-66(Ce). In addition, a higher amount HNO<sub>3</sub> favours the formation of F4_MIL-140A(Ce). Similarly, increasing the amount of AcOH leads to slowing down of the nucleation and growth rate, but favours the formation of F4_UiO-66(Ce). The pure F4_UiO-66(Ce) phase could also be obtained when using larger amounts of AcOH in the presence of minimal HNO<sub>3</sub>. Based on these <i>in situ</i> results, a new optimised route to achieving a pure, high quality F4_MIL-140A(Ce) phase in mild conditions (60 °C, 1 h) is also identified.


CrystEngComm ◽  
2020 ◽  
Vol 22 (47) ◽  
pp. 8182-8188
Author(s):  
Megan C. Wasson ◽  
Ken-ichi Otake ◽  
Xinyi Gong ◽  
Annabella R. Strathman ◽  
Timur Islamoglu ◽  
...  

Cerium-based metal–organic frameworks' crystal growth and structure dictated using modulating monocarboxylate species.


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