Nitrogen-Embedded Multi-Resonance Heteroaromatics with Prolonged Homogeneous Hexatomic Rings

被引:54
|
作者
Zeng, Xuan [1 ,2 ]
Wang, Xiang [1 ]
Zhang, Yuewei [1 ]
Meng, Guoyun [1 ]
Wei, Jinbei [3 ]
Liu, Ziyang [1 ]
Jia, Xiaoqin [1 ]
Li, Guomeng [1 ]
Duan, Lian [1 ,2 ]
Zhang, Dongdong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Organ Optoelect & Mol Engn Minist Educ De, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Ctr Flexible Elect Technol, Beijing 100084, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Res Educ Ctr Excellence Mol Sci, Inst Chem, Beijing 100190, Peoples R China
关键词
Bathochromic Shift; Device Stability; Homogeneous Hexatomic Rings; Multiple Resonance; Narrow Energy Gap; ACTIVATED DELAYED FLUORESCENCE; LIGHT; BORYLATION;
D O I
10.1002/anie.202117181
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrogen-containing polycyclic heteroaromatics have exhibited fascinating multi-resonance (MR) characteristics for efficient narrowband emission, but strategies to bathochromic shift their emissions while maintaining the narrow bandwidths remain exclusive. Here, homogeneous hexatomic rings are introduced into nitrogen-embedded MR skeletons to prolong the pi-conjugation length for low-energy electronic transitions while retaining the non-bonding character of the remaining parts. The proof-of-the-concept emitters exhibit near unity photoluminescence quantum yields with peaks at 598 nm and 620 nm and small full-width-at-half-maximums of 28 nm and 31 nm, respectively. Optimal organic light-emitting diodes exhibit a high external quantum efficiency of 18.2 %, negligible efficiency roll-off, and ultra-long lifetime with negligible degradation at an initial luminance of 10 000 cd m(-2) after 94 hours.
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页数:7
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