Spengler Jonas, Zhu Chongwei, Shoyama Kazutaka, Würthner Frank
Universität Würzburg, Institut für Organische Chemie and Center for Nanosystems Chemistry Am Hubland 97074 Würzburg Germany
Chem Sci. 2023 Sep 20;14(39):10861-10866. doi: 10.1039/d3sc04015a. eCollection 2023 Oct 11.
Aromatic dicarboximides are a class of molecules represented by the well-known rylene bis(dicarboximide)s, in particular perylene or naphthalene bis(dicarboximide)s, which show pronounced optoelectronic properties and are applied as color pigments, fluorescent dyes and organic semiconductors. Herein we extend the family of aromatic bis(dicarboximide)s and report the synthesis of the first series of non-alternant aromatic dicarboximides by twofold Pd-catalyzed [5 + 2] annulation. Characterization by UV/vis spectroscopy and cyclic voltammetry (CV) measurements give insight into the optoelectronic characteristics of the hitherto unexplored substance class of heptagon-containing imides. Theoretical studies by nucleus independent chemical shift (NICS) XY-scans and anisotropy of the induced current density (ACID) plots demonstrate the influence of both the non-alternant carbon framework and the imide moieties on aromaticity of the synthesized bisimides.
芳香族二羧酰亚胺是一类以著名的苝双(二羧酰亚胺)为代表的分子,特别是苝或萘双(二羧酰亚胺),它们表现出显著的光电性质,可用作彩色颜料、荧光染料和有机半导体。在此,我们扩展了芳香族双(二羧酰亚胺)家族,并报告了通过双重钯催化的[5 + 2]环化反应合成的第一系列非交替芳香族二羧酰亚胺。通过紫外/可见光谱和循环伏安法(CV)测量进行表征,深入了解了迄今未探索的含七元环酰亚胺物质类别的光电特性。通过核独立化学位移(NICS)XY扫描和感应电流密度各向异性(ACID)图进行的理论研究表明,非交替碳骨架和酰亚胺部分对合成的双酰亚胺的芳香性都有影响。