化学
酰胺
齿合度
铜
催化作用
组合化学
配体(生物化学)
联轴节(管道)
芳基
分子
荧光
二极管
光电子学
有机化学
金属
材料科学
受体
生物化学
烷基
物理
量子力学
冶金
作者
Sasa Li,Xia Huang,Yunlong Gao,Jian Jin
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-07-28
卷期号:24 (31): 5817-5824
被引量:9
标识
DOI:10.1021/acs.orglett.2c02364
摘要
Triarylamines are privileged core structures that are found in versatile optoelectronic materials. New methods are constantly being sought for their preparation. Herein, a new protocol for triarylamine synthesis is presented where a wide range of diarylamines couple smoothly with aryl bromides mediated by a copper oxalamide (or amide) catalytic system. Notably, a new non-C2-symmetric 1-isoquinolinamide-based N,N-/N,O-bidentate ligand was introduced that could tolerate bulky diarylamines. Plenty of known optoelectronic functional molecules could be synthesized in good to excellent yields. The practicality of this C-N cross-coupling was illustrated by the gram-scale synthesis of a patented thermally activated delayed fluorescence emitter for organic light-emitting diodes.
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