An investigation of palladium-catalyzed Stille-type cross-coupling of nitroarenes in perylenediimide series

被引：0
|
作者：
Makhloutah, Aline [1 ]
Hatych, Danylo [1 ]
Chartier, Thomas [1 ]
Rocard, Lou [1 ]
Goujon, Antoine [1 ]
Felpin, Francois-Xavier [2 ]
Hudhomme, Pietrick [1 ]
机构：
[1] Univ Angers, SFR Matrix, MOLTECH Anjou, CNRS, F-49000 Angers, France
[2] Univ Nantes, CEISAM, CNRS, UMR 6230, F-44000 Nantes, France
来源：
ORGANIC & BIOMOLECULAR CHEMISTRY | 2022年 / 20卷 / 02期
关键词：
ORGANIC SOLAR-CELLS; NON-FULLERENE ACCEPTOR; POLYMER; PERFORMANCE; LIGANDS;
D O I：
10.1039/d1ob02291a
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
We report herein an unprecedented palladium-catalyzed cross-coupling reaction between mononitro-perylenediimide (PDI) and various arylstannanes. Optimized conditions developed with this Stille-type reaction allow the grafting of (hetero)aryls of various electronic nature in the bay region of PDIs. Moreover, we capitalized on the high selectivity of this cross-coupling through the desymmetrization of the dinitro-PDI substrate.
引用
收藏
页码：362 / 365
页数：4
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