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碗状蒽稠合反芳香性镍(II)降卟啉:合成、结构、与碳的组装及光热转换

Bowl-Shaped Anthracene-Fused Antiaromatic Ni(II) Norcorrole: Synthesis, Structure, Assembly with C, and Photothermal Conversion.

作者信息

Wang Kaisheng, Ghosh Aninda, Shimizu Daiki, Takano Hideaki, Ishida Masatoshi, Kishi Ryohei, Shinokubo Hiroshi

机构信息

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.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 10;64(7):e202419289. doi: 10.1002/anie.202419289. Epub 2024 Nov 19.

Abstract

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.

摘要

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。

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