Wang Kaisheng, Ghosh Aninda, Shimizu Daiki, Takano Hideaki, Ishida Masatoshi, Kishi Ryohei, Shinokubo Hiroshi
Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi, 464-8603, Japan.
Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo, 192-0397, Japan.
Angew Chem Int Ed Engl. 2025 Feb 10;64(7):e202419289. doi: 10.1002/anie.202419289. Epub 2024 Nov 19.
The synthesis of bowl-shaped antiaromatic molecules is challenging because the molecular distortion further destabilizes these already inherently reactive molecules. Here, we report the synthesis and properties of bowl-shaped fused anthrylnorcorroles that exhibit near-infrared (NIR) absorption reaching 1900 nm. The oxidation of meso-anthryldibromodipyrrin provides fused anthryldibromodipyrrin, which was converted to the fused mono- and bisanthrylnorcorroles through Ni(0)-mediated intramolecular coupling with a bis(dibromodipyrrin) Ni(II) complex. Single-crystal X-ray diffraction analyses revealed bowl-shaped structures for the fused mono- and bisanthrylnorcorroles, which enables them to act as suitable receptors for C with bonding constants of 2.89×10 M and 1.59×10 M, respectively. The formation of a 1 : 1 complex between the fused monoanthrylnorcorrole and C was confirmed by single-crystal X-ray diffraction analysis. The effective expansion of the π-conjugation through the triple fusion of the norcorrole with the anthracene units substantially enhances the near-infrared absorption bands, which endows these anthrylnorcorroles with effective photothermal conversion.
碗状反芳香分子的合成具有挑战性,因为分子扭曲会进一步使这些本就固有反应性的分子变得不稳定。在此,我们报道了碗状稠合蒽基降卟啉的合成及其性质,其近红外(NIR)吸收可达1900 nm。中位蒽基二溴二吡咯的氧化生成了稠合蒽基二溴二吡咯,后者通过与双(二溴二吡咯)镍(II)配合物进行镍(0)介导的分子内偶联反应,转化为稠合单蒽基和双蒽基降卟啉。单晶X射线衍射分析揭示了稠合单蒽基和双蒽基降卟啉的碗状结构,这使得它们能够分别以2.89×10 M和1.59×10 M的结合常数作为合适的C受体。单晶X射线衍射分析证实了稠合单蒽基降卟啉与C之间形成了1 : 1配合物。通过降卟啉与蒽单元的三重稠合实现的π共轭有效扩展,显著增强了近红外吸收带,这赋予了这些蒽基降卟啉有效的光热转换能力。