Aromatic hydrocarbon macrocycles for highly efficient organic light-emitting devices with single-layer architectures
A modern electrophosphorescent organic light-emitting device (OLED) achieves quantitative electro-optical conversion by using multiple layers of molecular materials designed through role allotment for independent and specific functions. A unique, potentially innovative device architecture, i.e. , a...
Gespeichert in:
Veröffentlicht in: | Chemical science (Cambridge) 2016-01, Vol.7 (2), p.896-94 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | A modern electrophosphorescent organic light-emitting device (OLED) achieves quantitative electro-optical conversion by using multiple layers of molecular materials designed through role allotment for independent and specific functions. A unique, potentially innovative device architecture,
i.e.
, a single-layer phosphorescent OLED, is currently being developed by designing multirole base materials
via
a structural combination of multiple functional components in single molecules. The multirole molecules, however, inevitably require multiple processes to synthesize their multiple components and, moreover, to assemble these components synthetically into one molecule. We herein show that the multirole base material for a highly efficient single-layer phosphorescent OLED can be designed and synthesized with a single, very simple aromatic hydrocarbon component of toluene merely through a one-pot macrocyclization. Without requiring the assembly tasks at the synthesis stage, the molecular design allows for a concise one-pot synthesis of, and a quantitative electro-optical conversion in, the single-layer device architecture with a single-component base material.
Aromatic hydrocarbon macrocycles for phosphorescent organic light-emitting devices with a single-layer architecture were designed. |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c5sc03807c |