Yang Guang, Liu Kai-Yue, Cao Jing-Yi, Yu Jia-Ying, Sun De-Li, Wang Chuan-Zeng, Zhao Wen-Xuan, Elsegood Mark R J, Teat Simon J, Zhu Cheng-Chen, Yamato Takehiko
School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo 255049, PR China.
School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo 255049, PR China; Department of Applied Chemistry, Faculty of Science and Engineering, Saga University Honjo-machi 1, Saga 840-8502, Japan.
Spectrochim Acta A Mol Biomol Spectrosc. 2024 Jan 15;305:123529. doi: 10.1016/j.saa.2023.123529. Epub 2023 Oct 12.
Polycyclic aromatic hydrocarbon-fused [n]helicene derivatives (PAH-fused [n]helicenes) have been widely investigated due to their excellent photoelectric and chiroptical properties. Herein, a series of pyrene-fused helicenes were synthesized by a photocyclization reaction and characterized by H/C NMR spectroscopy and single crystal X-ray diffraction. All compounds and their vinyl precursors were studied as emitting materials. The experimental results reveal that these compounds possess reasonable emission efficiency (Φ = 97% for 3a) and tunable optical properties, and a wide emission band from bluish violet for 3c (401 nm) to green-yellow for 4c (530 nm) was observed. The detailed investigation indicated that an efficient, structure-controlled strategy was established to develop pyrene-based [n]helicene materials.
多环芳烃稠合的[n]螺旋烯衍生物(PAH稠合的[n]螺旋烯)因其优异的光电和手性光学性质而受到广泛研究。在此,通过光环化反应合成了一系列芘稠合螺旋烯,并通过H/C NMR光谱和单晶X射线衍射对其进行了表征。所有化合物及其乙烯基前体均作为发光材料进行了研究。实验结果表明,这些化合物具有合理的发光效率(3a的Φ = 97%)和可调谐的光学性质,并且观察到从3c(401 nm)的蓝紫色到4c(530 nm)的绿黄色的宽发射带。详细研究表明,已建立了一种高效、结构可控的策略来开发基于芘的[n]螺旋烯材料。