scholarly journals Hydrogen-Bonding Assembly of Coordination Polymers Showing Reversible Dynamic Solid-State Structural Transformations

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.

2017 ◽  
Vol 19 (40) ◽  
pp. 27516-27529 ◽  
Author(s):  
A. Kowalewska ◽  
M. Nowacka ◽  
M. Włodarska ◽  
B. Zgardzińska ◽  
R. Zaleski ◽  
...  

Thermally induced formation of symmetric crystal lattices in functional POSS proceeds via different mechanisms and results in unique reversible phenomena.


CrystEngComm ◽  
2020 ◽  
Vol 22 (5) ◽  
pp. 888-894 ◽  
Author(s):  
Ashkan Kianimehr ◽  
Kamran Akhbari ◽  
Jonathan White ◽  
Anukorn Phuruangrat

Two new Na and K coordination polymers with halogen bond, metallophilic and hydrogen bonding interactions were synthesized. These two compounds were synthesized sonochemically and solid-state conversions of them to each other were investigated.


2013 ◽  
Vol 19 (12) ◽  
pp. 3962-3968 ◽  
Author(s):  
Goutam Kumar Kole ◽  
Abdul Malik Puthan Peedikakkal ◽  
Belinda Mei Fang Toh ◽  
Jagadese J. Vittal

2017 ◽  
Vol 46 (48) ◽  
pp. 17025-17031 ◽  
Author(s):  
Xu-Feng Yang ◽  
Min Liu ◽  
Hai-Bin Zhu ◽  
Cheng Hang ◽  
Yue Zhao

Promoted by the DMF solvent, the 1D chain structure of 1 can be irreversibly transformed into the 3D sod network structure of 2 in a crystal-to-crystal fashion, which is accompanied by a drastic magnetic change.


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.


Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4088
Author(s):  
Javier Martí-Rujas

Thermal treatment is important in the solid-state chemistry of metal organic materials (MOMs) because it can create unexpected new structures with unique properties and applications that otherwise in the solution state are very difficult or impossible to achieve. Additionally, high-temperature solid-state reactivity provide insights to better understand chemical processes taking place in the solid-state. This review article describes relevant thermally induced solid-state reactions in metal organic materials, which include metal organic frameworks (MOFs)/coordination polymers (CPs), and second coordination sphere adducts (SSCs). High temperature solid-state reactivity can occur in a single-crystal-to-single crystal manner (SCSC) usually for cases where there is small atomic motion, allowing full structural characterization by single crystal X-ray diffraction (SC-XRD) analysis. However, for the cases in which the structural transformations are severe, often the crystallinity of the metal-organic material is damaged, and this happens in a crystal-to-polycrystalline manner. For such cases, in the absence of suitable single crystals, structural characterization has to be carried out using ab initio powder X-ray diffraction analysis or pair distribution function (PDF) analysis when the product is amorphous. In this article, relevant thermally induced SCSC reactions and crystal-to-polycrystalline reactions in MOMs that involve significant structural transformations as a result of the molecular/atomic motion are described. Thermal reactivity focusing on cleavage and formation of coordination and covalent bonds, crystalline-to-amorphous-to-crystalline transformations, host–guest behavior and dehydrochlorination reactions in MOFs and SSCs will be discussed.


RSC Advances ◽  
2014 ◽  
Vol 4 (33) ◽  
pp. 17265-17267 ◽  
Author(s):  
Lida Hashemi ◽  
Ali Morsali

Reversible anion-exchange of 2D lead(ii) coordination polymers from [Pb(4-bpdb)Br2]n (1) to [Pb(4-bpdb)Cl2]n (2) by solid state anion-replacement has been studied.


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