Tuning the Photophysical and Electrochemical Properties of Aza-Boron-Dipyridylmethenes for Fluorescent Blue OLEDs

A series of substituted aza-boron-dipyridylmethene (aD) compounds are demonstrated as fluorescent dopant emitters in blue organic light emitting diodes (OLEDs). Replacing the meso-carbon of a dipyridylmethene dye with nitrogen to form the aD chromophore leads to a destabilization of the highest occupied molecular orbital in aD, as evidenced both from their experimentally determined photophysical and electrochemical properties. These properties are consistent with theoretical calculations of the molecular energetics. These aD derivatives emit violet to blue light, peaking between 400 and 460 nm with photoluminescent quantum yields over 85%. The aD compounds have small energy differences (<400 meV) between their singlet and triplet excited states. OLEDs fabricated with an aza-boron-dipyridylmethene emitting fluorophore give an external quantum efficiency of 4.5% on glass substrates, close to the theoretical maximum for fluorescent OLEDs.

Automated summary

Substituted aza-boron-dipyridylmethene (aD) compounds have been demonstrated as efficient fluorescent dopant emitters in blue organic light emitting diodes (OLEDs), emitting violet to blue light with high photoluminescent quantum yields. The destabilization of the highest occupied molecular orbital in aD leads to small energy differences between their singlet and triplet excited states, contributing to the high external quantum efficiency of OLEDs with aza-boron-dipyridylmethene emitting fluorophores.