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Symmetrical versus asymmetrical molecular configuration in metal-assisted-through-space charge transfer TADF

  • Riga Technical University
  • University of Latvia

Research output: Chapter in Book/Report/Conference proceedingConference paperResearchpeer-review

1 Citation (Scopus)

Abstract

The synthesis of a novel imidazolidine type N-heterocyclic carbene (NHC) Cu (I) complex with asymmetrically attached phenylsulfonyl- acceptor group is presented. The asymmetrical ligand was used for the preparation two Cu(I) carbene-metal-amide (CMA) complexes with carbazolide (complex 1) or 1,8-dimethylcarbazolide (complex 2) as the amide donors. Obtained complexes exhibit efficient thermally activated delayed fluorescence (TADF) with luminescence quantum yields (QY) reaching 0.80 in PMMA matrix. Metal promoted through-space charge transfer approach in the emitter design lowers the ?EST gap and the small spin-orbit coupling (SOC) provided by metal atom enables high radiative rates (kr = 2.21×105 s-1 for complex 2). The photophysical properties of the asymmetrical (1-2) and previously reported symmetrical (3-6) molecular designs are compared. Obtained results suggest a closely similar photophysical behavior for both the asymmetrical and symmetrical CMA complexes.

Original languageEnglish
Title of host publicationOrganic Electronics and Photonics
Subtitle of host publicationFundamentals and Devices III
EditorsSebastian Reineke, Koen Vandewal, Wouter Maes
Volume12149
ISBN (Electronic)9781510651746
DOIs
Publication statusPublished - 2022

Publication series

NameProceedings of SPIE - The International Society for Optical Engineering
Volume12149
ISSN (Print)0277-786X
ISSN (Electronic)1996-756X

OECD Field of Science

  • 1.3 Physical Sciences

Keywords

  • carbene-metal-amides
  • N-heterocyclic carbenes
  • Thermally activated delayed fluorescence
  • through-space charge transfer

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