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Mechanical Force Induced Formation of Extrinsic Micropores in Coordination Polymers
Mechanical force can be employed not only to efficiently synthesize new materials under environmentally friendly conditions but also to change the macroscopic and microscopic properties of materials. Although coordination polymers (CPs) are attractive functional materials because they possess high s...
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Published in: | Inorganic chemistry 2022-02, Vol.61 (8), p.3379-3386 |
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container_title | Inorganic chemistry |
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creator | Noro, Shin-ichiro Zheng, Xin Wang, AnQi Suzuki, Kazushige Kosasang, Soracha Horike, Satoshi Padovan, Daniele Nakajima, Kiyotaka Sato, Hiroyasu Takahashi, Kiyonori Nakamura, Takayoshi |
description | Mechanical force can be employed not only to efficiently synthesize new materials under environmentally friendly conditions but also to change the macroscopic and microscopic properties of materials. Although coordination polymers (CPs) are attractive functional materials because they possess high structural designability and diversity, mechanical force-induced structural and functional changes of CPs are challenging issues. In this study, two one-dimensional CPs, one a densely packed nonporous CP [Cu2(bza)4(pyr)] (1) and the other a porous CP [Cu2(1-nap)4(pyr)] (2) (bza = benzoate, 1-nap = 1-naphthoate and pyr = pyrimidine), were subjected to ball-milling to assess the effect of mechanical force on their porosities. Ball mill treatments were found to induce an amorphization and cause a 30 fold enhancement of the CO2 adsorption amount at 195 K and P/P 0 ∼ 1 for 1 and a slightly decreased CO2 adsorption amount for 2. The results of thorough characterization studies suggest that the formation of extrinsic micropores in addition to extrinsic mesopores/macropores between particles takes place by ball milling. |
doi_str_mv | 10.1021/acs.inorgchem.1c02762 |
format | article |
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Although coordination polymers (CPs) are attractive functional materials because they possess high structural designability and diversity, mechanical force-induced structural and functional changes of CPs are challenging issues. In this study, two one-dimensional CPs, one a densely packed nonporous CP [Cu2(bza)4(pyr)] (1) and the other a porous CP [Cu2(1-nap)4(pyr)] (2) (bza = benzoate, 1-nap = 1-naphthoate and pyr = pyrimidine), were subjected to ball-milling to assess the effect of mechanical force on their porosities. Ball mill treatments were found to induce an amorphization and cause a 30 fold enhancement of the CO2 adsorption amount at 195 K and P/P 0 ∼ 1 for 1 and a slightly decreased CO2 adsorption amount for 2. 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title | Mechanical Force Induced Formation of Extrinsic Micropores in Coordination Polymers |
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