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1,5‐Diazocine‐Based Diaryl Ketones: Design, Synthesis, and Optoelectronic Properties.

Authors :
Sebastian, Anjitha
Darshan, Vibhu
Nharangatt, Bijoy
Maka, Vijay Kumar
Linet, Amrutham
Achankunju, Simi
Nagaoka, Masaki
Yagi, Shigeyuki
Unni K. N., Narayanan
Neogi, Ishita
Source :
Journal of Heterocyclic Chemistry; Dec2024, Vol. 61 Issue 12, p2040-2049, 10p
Publication Year :
2024

Abstract

Three novel heterocyclic host based on diaryl ketone‐tethered 1,5‐diazocines were designed and synthesized for applications in phosphorescent organic light‐emitting diodes (PhOLEDs). The hosts were derived by anchoring the naphthyl ketone (TBN), anthryl ketone (TBA), and phenanthryl ketone (TBP) to the 1,5‐diazocine core. The materials were successfully characterized using spectroscopic techniques. TBN and TBP exhibited low external quantum efficiency of 1.5% and 1.9% when explored as hosts in PhOLED devices. Among the series, TBP exhibited the highest luminance of 4160 cd/m2, maximum luminance efficiency of 6.3 cd/A, and power efficiency of 3.21 lm/w, when doped with Ir(ppy)3 in PhOLED. Nevertheless to our surprise, TBA manifested the lowest device performance than other TBs as a host due to low carrier mobility caused by a highly twisted structure as deciphered from the comparative analysis of single‐crystal structure that could impede carrier transport crucial for efficient electroluminescence. The outcomes of electroluminescence were validated and explained with analysis of single‐crystal structure, and also with the aid of density functional theory. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0022152X
Volume :
61
Issue :
12
Database :
Complementary Index
Journal :
Journal of Heterocyclic Chemistry
Publication Type :
Academic Journal
Accession number :
181439785
Full Text :
https://doi.org/10.1002/jhet.4915