发光
堆积
密度泛函理论
化学计量学
接受者
材料科学
上部结构
芘
电荷(物理)
化学
结晶学
化学物理
光电子学
物理
计算化学
物理化学
有机化学
地质学
海洋学
量子力学
凝聚态物理
作者
Bin Li,Lingling Liu,Yuan Wang,Kun Liu,Zhe Zheng,Shougang Sun,Yanan Hu,Liqiang Li,Chunju Li
标识
DOI:10.1038/s41467-024-46788-6
摘要
Organic co-crystals offer an opportunity to fabricate organic functional materials. Traditional co-crystals are generally packed following the segregated or mixed stacking mode, leading to the lack of structural and functional diversity. Herein, we report three sets of macrocycle co-crystals with identical co-constitutions. The macrocycle co-crystals differ in the stoichiometric ratios (2:1, 1:1, and 2:3) of the constituents and molecular packing modes. The co-crystals are constructed using triangular pyrene-macrocycle and 1,2,4,5-tetracyanobenzene exploiting exo-wall charge-transfer interactions. Interestingly, the three co-crystals exhibit distinct, tunable emission properties. The corresponding emission peaks appear at 575, 602, and 635 nm, covering yellow via orange to red. The X-ray diffraction analyses and the density functional theory calculations reveal the superstructure-property relationships that is attributed to the formation of different ratios of charge-transfer transition states between the donor and acceptor motifs, resulting in red-shifted luminescence.
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