Post-Modification of Pyrrolopyrrole Aza-BODIPY toward High Near-Infrared Fluorescence Brightness

被引:8
|
作者
Wang, Yitong [1 ,2 ,3 ]
Mori, Shigeki [1 ,2 ,3 ]
Nakanotani, Hajime [1 ,2 ,3 ]
Adachi, Chihaya [1 ,2 ,3 ]
Shimizu, Soji [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Appl Chem, Fukuoka, Fukuoka 8190395, Japan
[2] Ehime Univ, Adv Res Support Ctr ADRES, Matsuyama 7908577, Japan
[3] Kyushu Univ, Ctr Mol Syst CMS, Grad Sch Engn, Dept Appl Chem, Fukuoka 8190395, Japan
关键词
ABSORPTION; ANALOGS; DESIGN;
D O I
10.1021/acs.orglett.3c00848
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Pyrrolopyrrole aza-BODIPYs (PPABs), dimeric aza-BODIPY analogues, exhibit intense absorption and fluorescence in the visible and near-infrared (NIR) regions. Here, we developed a facile postmodification by palladium-catalyzed coupling reactions to synthesize a series of donor- acceptor-donor (D-A-D) PPABs. Despite the possible fluorescence quenching dictated by the energy-gap low, D-A-D PPABs exhibit high-fluorescence brightness in the NIR region, implying their potential use as a bright NIR emitter.
引用
收藏
页码:3040 / 3044
页数:5
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