堆积
多孔性
萘
聚合物
二亚胺
配体(生物化学)
电导率
晶体结构
金属有机骨架
丙酮
化学
材料科学
晶体工程
选择性
结晶学
超分子化学
分子
物理化学
有机化学
苝
受体
催化作用
复合材料
吸附
生物化学
作者
Ziqian Xue,Jia‐Jia Zheng,Yusuke Nishiyama,Ming‐Shui Yao,Yoshitaka Aoyama,Zeyu Fan,Ping Wang,T. Kajiwara,Yoshiki Kubota,Satoshi Horike,Ken‐ichi Otake,Susumu Kitagawa
标识
DOI:10.1002/ange.202215234
摘要
Abstract Exploring new porous coordination polymers (PCPs) that have tunable structure and conductivity is attractive but remains challenging. Herein, fine pore structure engineering by ligand conformation control of naphthalene diimide (NDI)‐based semiconducting PCPs with π stacking‐dependent conductivity tunability is achieved. The π stacking distances and ligand conformation in these isoreticular PCPs were modulated by employing metal centers with different coordination geometries. As a result, three conjugated PCPs (Co−pyNDI, Ni−pyNDI, and Zn−pyNDI) with varying pore structure and conductivity were obtained. Their crystal structures were determined by three‐dimensional electron diffraction. The through‐space charge transfer and tunable pore structure in these PCPs result in modulated selectivity and sensitivity in gas sensing. Zn−pyNDI can serve as a room‐temperature operable chemiresistive sensor selective to acetone.
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