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Effect of end group functionalisation of small molecules featuring the fluorene-thiophene-benzothiadiazole motif as emitters in solution-processed red and orange organic light-emitting diodes

  • Valentin H.K. Fell
  • , Neil J. Findlay*
  • , Benjamin Breig
  • , Clarissa Forbes
  • , Anto R. Inigo
  • , Joseph Cameron
  • , Alexander L. Kanibolotsky
  • , Peter J. Skabara
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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Abstract

A series of red fluorescent materials (compounds 1-4), which each contain the symmetric fluorene-thiophene-BT-thiophene-fluorene core, is presented along with their performance in solution-processed OLED devices. Extending the molecular conjugation through end-capping with additional fluorene units (compound 2), or through incorporation of donor functionalities (compounds 3 and 4) improves OLED performance relative to the parent compound 1. Notably, incorporating triphenylamine donor groups in compound 3 led to solution-processed OLED devices operating with a peak luminance of 2888 cd m −2 and a low turn-on voltage (3.6 V).

Original languageEnglish
Pages (from-to)3934-3944
Number of pages11
JournalJournal of Materials Chemistry C
Volume7
Issue number13
DOIs
Publication statusPublished - 4 Mar 2019

Funding

NJF, JC and AK thank the EPSRC for funding (EP/R03480X/1, EP/P02744X/2 and EP/N009908/2). We acknowledge the EPSRC UK National Mass Spectrometry Facility (NMSF) at Swansea University for HRMS data.

Keywords

  • end group functionalisation
  • small molecules
  • organic light-emitting diodes
  • fluorene–thiophene–benzothiadiazole motif

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