Synthesis of carbazole-fused azaborines via a Pd-catalyzed C-H activation-cyclization reaction

被引：0

作者：

Nagata M. ^{[1
]}

Oshiro T. ^{[2
]}

Mizuhata Y. ^{[2
]}

Tokitoh N. ^{[2
]}

Hosoya T. ^{[1
]}

Yamada S. ^{[3
]}

Konno T. ^{[3
]}

Fukumoto H. ^{[1
]}

Kubota T. ^{[1
]}

Agou T. ^{[1
]}

机构：

[1] Department of Quantum Beam Science, Graduate School of Science and Engineering, Ibaraki University, 4-12-1 Nakanarusawa, Hitachi, Ibaraki

[2] Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto

[3] Faculty of Molecular Chemistry and Engineering, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto

来源：

Bulletin of the Chemical Society of Japan | 2020年 / 94卷 / 01期

基金：

日本学术振兴会;

关键词：

Azaborines; C-H activation; Carbazole;

D O I：

10.1246/BCSJ.20200129

中图分类号：

学科分类号：

摘要：

Carbazole-fused azaborines were synthesized via a Buchwald-Hartwig amination followed by a Pd-catalyzed C-H activation-cyclization reaction. These azaborines exhibited red-shifted absorptions and photoluminescence emissions compared to those of dibenzoazaborines, suggesting the efficient HOMO-LUMO energy gap decrease by the carbazole-annulation. The carbazole-fused azaborines showed improved electrochemical stability compared with the previously reported dibenzoazaborine derivatives. © 2021 The Chemical Society of Japan

引用

页码：21 / 23

页数：2

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