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Highly Luminescent π-Conjugated Terpyridine Derivatives Exhibiting Thermally Activated Delayed Fluorescence.

Hisahiro SasabeYuya HayasakaRyutaro KomatsuKohei NakaoJunji Kido
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2016)
Typically, luminescent π-conjugated 2,2':6',2''-terpyridine (tpy) derivatives are versatile components for tridentate metal ligands, supramolecular materials, two-photon absorption bioimaging probes, fluorescent ion sensors, and organic light-emitting devices. However, a limited number of luminescent tpy materials, other than metal complexes, have been reported. This study introduces a series of π-conjugated tpy derivatives that exhibit strong thermally activated delayed fluorescence (TADF). We have observed that a blue tpy emitter outperforms conventional fluorescent emitters. Additionally, a green tpy emitter has exhibited a performance that is almost comparable to that of its green phosphorescent counterparts, realizing an external quantum efficiency close to 25 % and a power efficiency exceeding 80 lm W-1 with an exceptionally low efficiency roll-off. This study demonstrates the first example of highly luminescent tpy-based TADF emitters.
Keyphrases
  • light emitting
  • quantum dots
  • living cells
  • energy transfer
  • single molecule
  • photodynamic therapy
  • fluorescent probe
  • small molecule
  • molecular dynamics
  • low cost
  • metal organic framework
  • nucleic acid