Hydrogen-Bonding Assembly of Coordination Polymers Showing Reversible Dynamic Solid-State Structural Transformations
Autor: | Satoshi Kawata, Mariko Ishii, Shinya Hayami, Hitoshi Kumagai, Ken Kanazashi, Hisashi Konaka, Sadahiro Yagishita, Ryuta Ishikawa |
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Rok vydání: | 2018 |
Předmět: |
Materials science
Pyrazine Coordination polymer Hydrogen bond zinc Cationic polymerization metal-organic framework solid-state structural transformation 1D array cobalt Magnetic susceptibility lcsh:QD146-197 metal–organic framework Inorganic Chemistry coordination polymer Crystallography chemistry.chemical_compound chemistry lcsh:Inorganic chemistry pyrazine Molecule Metal-organic framework Powder diffraction |
Zdroj: | Inorganics, Vol 6, Iss 4, p 115 (2018) Inorganics Volume 6 Issue 4 |
ISSN: | 2304-6740 |
Popis: | 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&minus ) 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&minus (A), is an anionic infinite pyz bridged 1D array with chelating tdpd2&minus 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 crystallize in different crystal systems, powder X-ray diffraction (PXRD) measurements of the dehydrated forms, 1· 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. |
Databáze: | OpenAIRE |
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