Univ Lyon, Université Claude Bernard Lyon 1, INSA-Lyon, CPE-Lyon, ICBMS-UMR CNRS 5246, Campus Lyon-Tech la Doua, Bât. Lederer, 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne, France.
Chem Commun (Camb). 2018 Nov 15;54(92):12914-12929. doi: 10.1039/c8cc06403b.
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 π-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.
这篇专题文章总结了截至 2018 年文献中报道的[a]-苯并稠合 BODIPY 合成的不同策略。与传统的二/四氢异吲哚相比,这些π 扩展的 BODIPY 由于其在近红外区域的诱人光物理性质及其更高的(光)化学稳定性,是生物成像和有机光伏应用中很有前途的荧光团。本文综述中描述的四个主要策略可用于直接获得预期的[a]-苯并稠合 BODIPY,也可通过二/四氢异吲哚获得。