4.7 Article

Synthesis and Functionalization of Asymmetrical Benzo-Fused BODIPY Dyes

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 75, 期 17, 页码 6035-6038

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo101164a

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资金

  1. National Nature Science Foundation of China [20802002, 20902004]
  2. Anhui Province [090416221, KJ2009A 130]
  3. Scientific Research Foundation Ministry
  4. Ministry of Education of China [2009342120001]

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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.

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