Sonoda Yoriko, Tohnai Norimitsu, Shimoi Yukihiro
Research Institute for Advanced Electronics and Photonics, National Institute of Advanced Industrial Science and Technology, Higashi 1-1-1, Tsukuba, Ibaraki, 305-8565, Japan.
Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka, 565-0871, Japan.
Chempluschem. 2020 Sep;85(9):1968-1980. doi: 10.1002/cplu.202000285. Epub 2020 Aug 3.
Crystal structures and fluorescence spectroscopic properties were investigated for a series of all-(E) α,ω-di(4-pyridyl)polyenes (1-5) with different number of double bonds (n). Molecules 1 and 2 (n=1, 2) in crystals are arranged to form partially π-overlapped structures, whereas those of 3-5 (n=3-5) are stacked in a herringbone fashion. All these molecules, the shorter polyenes in particular, are almost nonfluorescent in solution. In the solid state, 1 and 2 are highly emissive as pure organic solids [fluorescence quantum yields (φ )=0.3-0.5], while 3 and 4 are only weakly fluorescent (φ <0.05). The strongly n-dependent fluorescence properties can be attributed to the largely different molecular arrangements in the crystals. Although 5 is nonfluorescent in the solid state, we observe a very clear structure-property relationship in 1-4. Compounds 1 and 2 become much more emissive in the solid state than in solution as a result of the aggregation-induced emission (AIE) effect.
研究了一系列具有不同双键数目(n)的全(E)式α,ω-二(4-吡啶基)多烯(1-5)的晶体结构和荧光光谱性质。晶体中的分子1和2(n = 1, 2)排列形成部分π-重叠结构,而分子3-5(n = 3-5)则以人字形方式堆积。所有这些分子,特别是较短的多烯,在溶液中几乎不发荧光。在固态下,1和2作为纯有机固体具有高发射性[荧光量子产率(φ)= 0.3 - 0.5],而3和4仅具有弱荧光(φ < 0.05)。强烈的n依赖性荧光性质可归因于晶体中分子排列的很大差异。尽管5在固态下不发荧光,但我们在1-4中观察到非常明确的结构-性质关系。由于聚集诱导发光(AIE)效应,化合物1和2在固态下比在溶液中发射性更强。