Molecular Design and Function Group, National Institute for Materials Science (NIMS), 1-2-1 Sengen, Tsukuba 305-0047, Japan.
Department of Chemistry, Faculty of Pure & Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8477, Japan.
J Am Chem Soc. 2021 Mar 3;143(8):3238-3244. doi: 10.1021/jacs.0c13389. Epub 2021 Feb 18.
We report herein the solution and solid-state studies of conformationally flexible multidecker naphthalenediimides (NDIs) in which the chromophoric NDI units intramolecularly assemble into a series of discrete π-stacks. The X-ray crystallography reveals the existence of exclusively all- NDIs orientations in lower congeners while in a higher congener, suggesting short- to long-range π···π interactions throughout the slipped π chromophoric array. The UV/vis and fluorescence spectra evaluate the discrete π-stacks by remarkable optical changes upon cooling in solution. Furthermore, we carried out a systematic electrochemical investigation to gain an insight into redox properties of the long-range π-stacked structures. The higher congener () shows a ten-electron reversible reduction process in a small working potential window (∼0.8 V). To our knowledge, this is an unusual observation in an organic molecular system to undergo up to ten-electron reduction. These results pave the way to design multidecker π-stacks in which structural control with specific electronic properties would be engineered.
我们在此报告了构象柔性多并苯二酰亚胺(NDIs)的溶液和固态研究,其中发色团 NDI 单元在分子内组装成一系列离散的π-堆叠。X 射线晶体学揭示了在低同系物中仅存在全 NDI 取向,而在较高同系物中,表明在滑动的π发色团阵列中存在短程至远程π···π相互作用。紫外/可见和荧光光谱通过在溶液中冷却时显著的光学变化来评估离散的π-堆叠。此外,我们进行了系统的电化学研究,以深入了解长程π堆叠结构的氧化还原性质。较高同系物()在较小的工作电位窗口(约 0.8 V)中显示出十个电子的可逆还原过程。据我们所知,这在有机分子体系中是一个不寻常的观察结果,可以进行多达十个电子的还原。这些结果为设计多并苯π-堆叠铺平了道路,在这种堆叠中可以控制结构并具有特定的电子性质。