Flexibility Control of Two‐Dimensional Coordination Polymers by Crystal Morphology: Water Adsorption and Thermal Expansion
Flexibility Control of Two‐Dimensional Coordination Polymers by Crystal Morphology: Water Adsorption and Thermal Expansion
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通过晶体形态控制二维配位聚合物的柔性:水吸附和热膨胀
DOI:
10.1002/chem.202103404
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Ohba Masaaki
中科院分区:
文献类型:
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作者:
Ohtani Ryo;Yoshino Haruka;Yanagisawa Junichi;Ohtsu Hiroyoshi;Hashizume Daisuke;Hijikata Yuh;Pirillo Jenny;Sadakiyo Masaaki;Kato Kenichi;Shudo Yuta;Hayami Shinya;Le Ouay Benjamin;Ohba Masaaki
Layer flexibility in two‐dimensional coordination polymers (2D‐CPs) contributes to several functional materials as it results in anisotropic structural response to external stimuli. Chemical modification is a common technique for modifying layer structures. This study demonstrates that crystal morphology of a cyanide‐bridged 2D‐CP of type [Mn(salen)]2[ReN(CN)4] (1) consisting of flexible undulating layers significantly impacts the layer configuration and assembly. Nanoplates of1showed an in‐plane contraction of layers with a longer interlayer distance compared to the micrometer‐sized rod‐type particles. These effects by crystal morphology on the structure of the 2D‐CP impacted the structural flexibility, resulting in dual‐functional changes: the enhancement of the sensitivity of structural transformation to water adsorption and modification of anisotropic thermal expansion of1. Moreover, the nanoplates incorporated new adsorption sites within the layers, resulting in the uptake of an additional water molecule compared to the micrometer‐sized rods.