化学
系统间交叉
蒽
配体(生物化学)
光化学
荧光
位阻效应
金属有机骨架
金属
兴奋剂
电子转移
立体化学
物理化学
有机化学
单重态
激发态
吸附
受体
物理
核物理学
量子力学
生物化学
光电子学
作者
Zhiye Wang,Bingling Dai,Yuming Su,Huihui Hu,Xinru He,Jiawei Chen,Cheng Wang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-07-19
卷期号:62 (30): 11809-11816
被引量:7
标识
DOI:10.1021/acs.inorgchem.3c01036
摘要
Metal-organic frameworks (MOFs) built from fluorescent ligands frequently exhibit enhanced fluorescence when doped with inert ligands. This study focuses on a MOF of the UiO-68 structure, which is built from a fluorescent dibenzoate-anthracene ligand doped with a dibenzoate-benzene ligand. Our investigation aims to understand the mechanism behind the doping-enhanced emission of this MOF. We rule out several possible mechanisms, including exciton coupling, electron transfer between ligand and metal center, and ligand intersystem crossing induced by the metal center. Inhibition of the interligand charge transfer is considered a possible way to enhance emission. Furthermore, we propose that the conformational change of the anthracene-based ligand in the MOF cavity is also a way for enhancement. Our molecular dynamics simulations of the MOF structure filled with solvents reveal that the steric crowding in the cavity induces a conformational change at different doping levels, affecting the rate of intersystem crossing of the ligand.
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