Sterically Protected N2O-Type Benzopyrromethene Boron Complexes from Boronic Acids with Intense Red/Near-Infrared Fluorescence

被引:50
作者
Chen, Na [1 ]
Zhang, Wenjie [3 ]
Chen, Shun [3 ]
Wu, Qinghua [1 ]
Yu, Changjiang [1 ]
Wei, Yun [1 ]
Xu, Yuekang [3 ]
Hao, Erhong [1 ]
Jiao, Lijuan [2 ]
机构
[1] Anhui Normal Univ, Minist Educ, Lab Funct Mol Solids, Wuhu 241000, Peoples R China
[2] Anhui Normal Univ, Sch Chem & Mat Sci, Wuhu 241000, Peoples R China
[3] Anhui Normal Univ, Sch Life Sci, Wuhu 241000, Peoples R China
关键词
BODIPY DYES; SPECTROSCOPIC PROPERTIES; DIPYRROMETHENES BODIPYS; PHOTODYNAMIC THERAPY; HIGHLY FLUORESCENT; FUSED BODIPY; FAR-RED; MITOCHONDRIA; PROBES; BORONDIPYRROMETHENE;
D O I
10.1021/acs.orglett.7b00601
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of N2O-type benzopyrromethene boron complexes have been synthesized from the condensation of pyrrole, formylisoindole, and various boronic acids. These dyes have red/near-infrared absorption, high solution- and solid-state fluorescence, as well as good solubility in a variety of solvents due to the presence of axial-substituted groups that provide steric protection and prevent their possible aggregations. Two water-soluble derivatives with pyridinium ions were developed as near-infrared excitable mitochondrially localizing fluorescent probes.
引用
收藏
页码:2026 / 2029
页数:4
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