三聚体
四硫富瓦烯
离域电子
金属有机骨架
光化学
热稳定性
未成对电子
X射线光电子能谱
分子内力
电子顺磁共振
吸收(声学)
激进的
结晶学
化学
材料科学
物理化学
有机化学
分子
二聚体
核磁共振
吸附
复合材料
物理
作者
Jian Su,Ning Xu,Ryuichi Murase,Zhimei Yang,Deanna M. D’Alessandro,Jing‐Lin Zuo,Jia Zhu
标识
DOI:10.1002/anie.202013811
摘要
Abstract A series of stable radical 2D metal‐organic frameworks has been assembled. ( m ‐TTFTB) 3 ( m ‐Tetrathiafulvalene‐tetrabenzoate) trimer building blocks are beneficial for the stability of the radicals due to delocalization of the unpaired electron. Hexanuclear rare‐earth‐cluster‐based 1D chains further enhance the stability of the frameworks. The radical state of the middle TTF in the trimer has been observed by the change of central C−C and C−S bond distances and the configuration of the TTF by single‐crystal X‐ray diffraction. The radical characteristics are also confirmed by electron paramagnetic resonance, UV/Vis–NIR absorption, and X‐ray photoelectron spectroscopy experiments. Stability tests showed that the radicals are stable even in solutions and under acid/base environments (pH 1–12). Owing to efficient light absorption due to intramolecular charge transfer, low thermal conductivity, and outstanding stability, the radical 2D Dy‐MOF shows excellent photothermal properties, an increase of 34.7 °C within 240 s under one‐sun illumination.
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