Synthesis and Functionalization of Asymmetrical Benzo-Fused BODIPY Dyes

被引:101
|
作者
Jiao, Lijuan [1 ]
Yu, Changjiang
Liu, Mingming
Wu, Yangchun
Cong, Kebing
Meng, Ting
Wang, Yuqing
Hao, Erhong
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Key Lab Funct Mol Solids, Wuhu 241000, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2010年 / 75卷 / 17期
关键词
FLUORESCENCE QUANTUM YIELDS; RESONANCE ENERGY-TRANSFER; RESTRICTED AZA-BODIPY; NEAR-INFRARED NIR; BORON-DIPYRROMETHENE; LIVING CELLS; DISTYRYL-BORADIAZAINDACENES; SPECTROSCOPIC PROPERTIES; HIGHLY FLUORESCENT; VISIBLE-LIGHT;
D O I
10.1021/jo101164a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of asymmetrical benzo-fused BODIPY dyes were synthesized from the Sonogashira coupling and nucleophilic substitution reactions on the 3-halogenated benzo-fused BODIPY, generated from readily available 3-halogeno-1-formylisoindoles in a two-step synthetic procedure. This novel BODIPY platform provides an easy path for the linking of BODIPY fluorophore to various desired functionalities as demonstrated in this work. Most of the resulting BODIPY dyes show long-wavelength absorption and fluorescence emission, with good fluorescence quantum yields and long fluorescence lifetimes.
引用
收藏
页码:6035 / 6038
页数:4
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