Recent advances in the synthesis of [a]-benzo-fused BODIPY fluorophores

被引：86

作者：

Jean-Gerard, Ludivine ^{[1
]}

Vasseur, William ^{[1
,2
]}

Scherninski, Francois ^{[2
]}

Andrioletti, Bruno ^{[1
]}

机构：

[1] Univ Claude Bernard Lyon 1, Univ Lyon, INSA Lyon, CPE Lyon,ICBMS,CNRS,UMR 5246, Campus Lyon Tech Doua,43 Blvd 11 Novembre 1918, F-69622 Villeurbanne, France

[2] Labs Synth Innov, 2 Bis Rue Dupont Eure, F-75020 Paris, France

来源：

CHEMICAL COMMUNICATIONS | 2018年 / 54卷 / 92期

关键词：

NEAR-INFRARED FLUOROPHORES; SEMICONDUCTING POLYMER DOTS; SENSITIZED SOLAR-CELLS; WATER-SOLUBLE BODIPY; AZA-BODIPY; BORON-DIPYRROMETHENES; SPECTROSCOPIC PROPERTIES; PHOTODYNAMIC THERAPY; SPECTRAL PROPERTIES; ORGANIC PHOTOVOLTAICS;

D O I：

10.1039/c8cc06403b

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

This feature article summarizes the different strategies for the synthesis of [a]-benzo-fused BODIPYs that have been reported in the literature until 2018. These -extended BODIPYs are promising fluorophores for bio-imaging and organic photovoltaic applications due to both their attractive photophysical properties in the near-infrared area and their higher (photo)chemical stability compared to conventional bis-styryl derivatives. The four main strategies described in this review can be used to access either directly the expected [a]-benzo-fused BODIPYs or through the di-/tetra-hydroisoindole.

引用

页码：12914 / 12929

页数：16

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