电荷(物理)
传输(计算)
空格(标点符号)
化学物理
材料科学
纳米技术
化学
物理
计算机科学
量子力学
并行计算
操作系统
作者
Yang‐Kun Qu,Dong‐Ying Zhou,Qi Zheng,Peng Zuo,Zong‐Lu Che,Liang‐Sheng Liao,Zuo‐Quan Jiang
标识
DOI:10.1002/anie.202408712
摘要
Noncovalent spatial interaction has become an intriguing and important tool for constructing optoelectronic molecules. In this study, we linearly attached three conjugated units in a multi π-stacked manner by using just one trident bridge based on indeno[2,1-b]fluorene. To achieve this structure, we improved the synthetic approach through double C-H activation, significantly simplifying the preparation process. Due to the proximity of the C10, C11, and C12 sites in indeno[2,1-b]fluorene, we derived two novel donor|acceptor|donor (D|A|D) type molecules, 2DMB and 2DMFB, which exhibited closely packed intramolecular stacking, enabling efficient through-space charge transfer. This molecular construction is particularly suitable for developing high-performance thermally activated delayed fluorescence materials. With donor(s) and acceptor(s) constrained and separated within this spatially rigid structure, elevated radiative transition rates, and high photoluminescence quantum yields were achieved. Organic light-emitting diodes incorporating 2DMB and 2DMFB demonstrated superior efficiency, achieving maximum external quantum efficiencies of 28.6% and 16.2%, respectively.
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