化学
苯并咪唑
金属有机骨架
皮秒
接受者
配体(生物化学)
组合化学
光谱学
超短脉冲
吸收光谱法
光化学
拓扑(电路)
能量转移
纳米技术
化学物理
物理化学
有机化学
光学
激光器
生物化学
物理
受体
数学
材料科学
吸附
量子力学
组合数学
凝聚态物理
作者
Jiangtao Jia,Luis Gutiérrez‐Arzaluz,Osama Shekhah,Norah Alsadun,Justyna Czaban‐Jóźwiak,Sheng Zhou,Osman M. Bakr,Omar F. Mohammed,Mohamed Eddaoudi
摘要
Herein, we report a new light-harvesting mixed-ligand Zr(IV)-based metal-organic framework (MOF),with underlying fcu topology, encompassing the [Zr6(μ3-O)4(μ3-OH)4(O2C-)12] cluster and an equimolar mixture of thiadiazole- and benzimidazole-functionalized ligands. The successful integration of ligands with similar structural features but with notable chemical distinction afforded the attainment of a highly efficient energy transfer (ET). Notably, the very strong spectral overlap between the emission spectrum of benzimidazole (energy donor) and the absorption spectrum of thiadiazole (energy acceptor) provided an ideal platform to achieve very rapid (picosecond time scale) and highly efficient energy transfer (around 90% efficiency), as evidenced by time-resolved spectroscopy. Remarkably, the ultrafast time-resolved experiments quantified for the first time the anticipated close proximity of the two linkers with an average distance of 17 Å. This finding paves the way for the design and synthesis of periodic MOFs affording very efficient and fast ET to mimic natural photosynthetic systems.
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