分子内力
反铁磁性
分子间力
金属有机骨架
阳离子聚合
电子顺磁共振
二聚体
未成对电子
吸附
顺磁性
半导体
化学
铜
材料科学
光化学
分子
物理化学
核磁共振
立体化学
凝聚态物理
高分子化学
有机化学
光电子学
物理
作者
Xiang Xue,Zheng Liu,Jinghang Wang,Hewen Liu
标识
DOI:10.1063/1674-0068/cjcp2109178
摘要
Metal-organic frameworks (MOFs) draw more and more attentions due to their abundant properties and potential applications in materials science. Developing new MOFs structures often gets unexpected material properties. Herein, we report the properties of a copper [2,2]paracyclophane dicarboxylate MOF (CuCP-MOF). The magnetic properties of both CuCP-MOF and activated CuCP-MOF are investigated. CuCP-MOF shows the triplet state electron paramagnetic resonance spectrum at room temperature due to the antiferromagnetic coupling of the copper(II) paddlewheel (Cu-PW) dimer centers. The MOF has strong intramolecular antiferromagnetic interactions (inside the paddle-wheel dimer centers) and very weak intermolecular interactions, while activated CuCP-MOF exhibits strong intramolecular and intermolecular interactions due to the existence of unpaired Cu(II) centers. We also investigate the electronic structure and semiconductor behavior of CuCP-MOF. The MOF is assigned to direct bandgap semiconductors. Moreover, CuCP-MOF could selectively adsorb cationic organic dyes. By utilizing the synergistic effects on adsorption and photodegradation, we successfully apply CuCP-MOF to organic dye removal.
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