Meso-substituted boron-dipyrromethene compounds: synthesis, tunable solid-state emission, and application in blue-driven LEDs

Luminescence. 2021 Nov;36(7):1697-1705. doi: 10.1002/bio.4111. Epub 2021 Jul 6.

Abstract

In this work, we depict the synthesis and characterization of a series of meso-substituted boron-dipyrromethene (BODIPY) compounds. Their optical and electrochemical properties were investigated systematically. All these compounds exhibited intense absorption bands in the ultraviolet (UV) and visible regions, which arise from the π-π* transitions based on their BODIPY core segments. By comparing electron-withdrawing substituents and electron-donating substituents, we found that these compounds exhibited some similar photophysical properties but exhibited different fluorescence in the solid state. All compounds were highly emissive in dichloromethane at room temperature (λem = 512-523 nm, ΦPL > 0.9). When these compounds were applied in blue-driven light-emitting diodes (LEDs) as light-emitting materials, the devices showed luminescence efficiency ranging from 1.09 to 34.13 lm/W. Their luminescence and electrochemical properties could be used for understanding the structure-property relationship of BODIPY compounds and developing functional fluorescent materials.

Keywords: BODIPY; electrochemical properties; emission; light-emitting diodes; synthesis.

MeSH terms

  • Boron Compounds
  • Boron*
  • Luminescence
  • Porphobilinogen* / analogs & derivatives

Substances

  • Boron Compounds
  • dipyrromethene
  • Porphobilinogen
  • Boron