A Theoretical Design of Chiral Molecules through Conformational Lock towards Circularly Polarized Luminescence

被引:0
作者
Wang, Lewen [1 ]
He, Tengfei [2 ]
Liao, Hailiang [1 ]
Luo, Yige [1 ]
Ou, Wen [1 ]
Yu, Yinye [1 ,3 ,4 ]
Yue, Wan [1 ]
Long, Guankui [2 ]
Wei, Xingzhan [3 ]
Zhou, Yecheng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, Guangzhou Key Lab Flexible Elect Mat & Wearable D, Guangzhou 510006, Peoples R China
[2] Nankai Univ, Renewable Energy Convers & Storage Ctr RECAST, Natl Inst Adv Mat, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[3] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Micronano Mfg & Syst Integrat Ctr, Chongqing 400714, Peoples R China
[4] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
circularly polarized luminescence; chirality transformation; light emission; conformation lock; density functional theory; ELECTROLUMINESCENCE; POLYMER; METAL;
D O I
10.3390/photonics9080532
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Circularly polarized (CP) light has shown great potential in quantum computing, optical communications, and three-dimensional displays. It is still a challenge to produce high-efficiency and high-purity CP light. Herein, we proposed a strategy to design chiral organic small molecules for CP light generation. These kinds of chiral molecules are formed by achiral light-emitting groups and achiral alkyl chains through conformational lock, which indicates that chirality can also be introduced into achiral light-emitting groups through rational molecular design. The chirality of these molecules can be further tuned by changing the length of the alkyl chains connecting the diketopyrrolopyrrole unit. The chiroptical properties of these molecules are confirmed by calculated electronic circular dichroism and chiral emission spectra, and further confirmed in experiments. The strategy developed in this work will greatly enlarge the candidate library of chiral luminescent materials.
引用
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页数:10
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