Probing Solid-State Breathing and Structural Transformations in a Series of Silver(I) Porous Coordination Polymers

2015 ◽  
Vol 2015 (22) ◽  
pp. 3723-3729 ◽  
Author(s):  
Witold M. Bloch ◽  
Christopher J. Sumby
2013 ◽  
Vol 19 (12) ◽  
pp. 3962-3968 ◽  
Author(s):  
Goutam Kumar Kole ◽  
Abdul Malik Puthan Peedikakkal ◽  
Belinda Mei Fang Toh ◽  
Jagadese J. Vittal

CrystEngComm ◽  
2015 ◽  
Vol 17 (8) ◽  
pp. 1839-1847 ◽  
Author(s):  
Meng Kang ◽  
Guo-Ping Yang ◽  
Lei Hou ◽  
Wei-Ping Wu ◽  
Yun-Long Wu ◽  
...  

Four multi-dimensional nickel-based coordination polymers have been prepared, and their solvent-mediated and solid-state structural transformations have been observed and studied systematically.


CrystEngComm ◽  
2015 ◽  
Vol 17 (44) ◽  
pp. 8388-8413 ◽  
Author(s):  
Biswajit Bhattacharya ◽  
Debajyoti Ghoshal

Mixed ligand metal–organic frameworks (MOFs) have resolutely established themselves as a class of excellent solid state sorbents for carbon dioxide (CO2) and a proper design of such MOF can potentially improve not only the amount of CO2 adsorption, but also the selectivity of CO2 uptake over other gases and volatiles.


Inorganics ◽  
2018 ◽  
Vol 6 (4) ◽  
pp. 115
Author(s):  
Hitoshi Kumagai ◽  
Sadahiro Yagishita ◽  
Ken Kanazashi ◽  
Mariko Ishii ◽  
Shinya Hayami ◽  
...  

We herein report the synthesis, single-crystal structures of coordination polymers, and structural transformations of complexes employing 1,4,5,6-tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile (tdpd2−) and pyrazine (pyz) as bridging ligands. {[M(H2O)4(pyz)][M(tdpd)2(pyz)]·6(H2O)}n, [1·10H2O and 2·10H2O where M = Co (1) and Zn (2)], consists of two types of crystallographically independent one-dimensional (1D) structures packed together. One motif, [M(tdpd)2(pyz)]2− (A), is an anionic infinite pyz bridged 1D array with chelating tdpd2− ligands, and the other motif is a cationic chain, [M(H2O)4(pyz)]2+ (B), which is decorated with four terminal water molecules. The 1D arrays (A) and (B) are arranged in parallel by multi-point hydrogen-bonding interactions in an alternate (A)(B)(A)(B) sequence extending along the c-axis. Both compounds exhibit structural transformations driven by thermal dehydration processes around 350 K to give partially dehydrated forms, 1·2H2O and 2·2H2O. The structural determination of the partially dehydrated form, 2·2H2O, reveals a solid-state structural transformation from a 1D chain structure to a two-dimensional (2D) coordination sheet structure, [Zn2(tdpd)2(H2O)2(pyz)]n (2·2H2O). Further heating to 500 K yields the anhydrous form 2. While the virgin samples of 1·10H2O and 2·10H2O crystallize in different crystal systems, powder X-ray diffraction (PXRD) measurements of the dehydrated forms, 1·2H2O and 2·2H2O, are indicative of the same structure. The structural transformation is irreversible for 1·10H2O at ambient conditions. On the other hand, compound 2·10H2O shows a reversible structural change. The solid-state structural transformation for 1·10H2O was also confirmed by monitoring in-situ magnetic susceptibility, which is consistent with other thermally-induced measurements.


2019 ◽  
Vol 19 (4) ◽  
pp. 2235-2244 ◽  
Author(s):  
Cheng-Peng Li ◽  
Jin-Yun Ai ◽  
Hongming He ◽  
Ming-Ze Li ◽  
Miao Du

2013 ◽  
Vol 19 (12) ◽  
pp. 4080-4080 ◽  
Author(s):  
Goutam Kumar Kole ◽  
Abdul Malik Puthan Peedikakkal ◽  
Belinda Mei Fang Toh ◽  
Jagadese J. Vittal

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