Synthesis of Hexaazatruxenes by Consecutive N-H/C-H Coupling Using a Hypervalent Iodine Reagent and Evaluation of Their Photophysical Properties

被引:0
|
作者
Wu, Yuchen [1 ]
Sasayama, Takuma [1 ]
Gotoh, Takahiro [2 ]
Ito, Mamoru [1 ]
Shibata, Takanori [1 ]
机构
[1] Waseda Univ, Sch Adv Sci & Engn, Dept Chem & Biochem, Shinjuku Ku, Tokyo 1698555, Japan
[2] Waseda Univ, Mat Characterizat Cent Lab, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
关键词
Hypervalent compounds; Nitrogen heterocycles; Photoirradiation; Truxenes; TRUXENE; ANALOGS; BLUE;
D O I
10.1002/ejoc.202200438
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Truxene is a C-3-symmetric compound with characteristic photophysical properties, and it has great potential as a light-emitting material and building block. In this study, we demonstrate the synthesis of hexaazatruxenes using a two-step protocol. First, the hexaazatruxene precursors were prepared through the Buchwald-Hartwig amination of 1,3,5-tribromobenzene with commercially available or easily prepared amino-pyridine derivatives. Then, hexaazatruxenes were synthesized through consecutive N-H/C-H coupling using a hypervalent iodine reagent. To the best of our knowledge, this is the first report on the synthesis of truxenes containing more than three heteroatoms in the main skeleton.
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页数:6
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