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Organoboron-based multiple-resonance emitters: synthesis, structure-property correlations, and prospects.
Mamada, Masashi; Hayakawa, Masahiro; Ochi, Junki; Hatakeyama, Takuji.
Afiliação
  • Mamada M; Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan. hatake@kuchem.kyoto-u.ac.jp.
  • Hayakawa M; Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan. hatake@kuchem.kyoto-u.ac.jp.
  • Ochi J; Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan. hatake@kuchem.kyoto-u.ac.jp.
  • Hatakeyama T; Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan. hatake@kuchem.kyoto-u.ac.jp.
Chem Soc Rev ; 53(3): 1624-1692, 2024 Feb 05.
Article em En | MEDLINE | ID: mdl-38168795
ABSTRACT
Boron-based multiple-resonance (MR) emitters exhibit the advantages of narrowband emission, high absolute photoluminescence quantum yield, thermally activated delayed fluorescence (TADF), and sufficient stability during the operation of organic light-emitting diodes (OLEDs). Thus, such MR emitters have been widely applied as blue emitters in triplet-triplet-annihilation-driven fluorescent devices used in smartphones and televisions. Moreover, they hold great promise as TADF or terminal emitters in TADF-assisted fluorescence or phosphor-sensitised fluorescent OLEDs. Herein we comprehensively review organoboron-based MR emitters based on their synthetic strategies, clarify structure-photophysical property correlations, and provide design guidelines and future development prospects.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article