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Highly Linearized Twisted Iridium(III) Complexes.

Ross J DavidsonYu-Ting HsuGareth C GriffithsChenfei LiDmitry YufitRobert PalAndrew Beeby
Published in: Inorganic chemistry (2018)
Improving the spatial alignment of emitting molecules has long been a goal of organic-light-emitting-diode development to improve device efficiencies and to generate polarized emission. Herein we describe a simple approach employing Sonogashira coupling with alkyne iridium(phenylpyridine)2(acetylacetone) synthons (2-5) to generate eight linear iridium complexes (6-13) with crystallographically determined lengths of up to 5 nm. By embedding these "long" complexes into a polymer matrix and stretching it, an improvement of the polarization ratio of unstretched and stretched films of up to 7.1 times was achieved. Additionally, through the inclusion of "twists" in the complexes, the electronic coupling between the iridium center and substituent was controlled, giving a system where the emission behavior is independent of the length.
Keyphrases
  • light emitting
  • room temperature
  • photodynamic therapy
  • ionic liquid
  • carbon nanotubes
  • solid state
  • transition metal