Related Experiment Video
Updated: Aug 9, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Isomeric thermally activated delayed fluorescence emitters for highly efficient organic light-emitting diodes
Yanyan Liu1, Jiaji Yang2, Zhu Mao3
1PCFM Lab, GDHPPC Lab, Guangdong Engineering Technology Research Center for High-performance Organic and Polymer Photoelectric Functional Films, State Key Laboratory of OEMT, School of Chemistry, Sun Yat-sen University Guangzhou 510275 China chizhg@mail.sysu.edu.cn.
Abstract:
The isomeric strategy is an important design concept in molecular design that has a non-negligible influence on molecular properties. Herein, two isomeric thermally activated delayed fluorescence (TADF) emitters (NTPZ and TNPZ) are constructed with the same skeleton consisting of an electron donor and electron acceptor but different connection sites. Systematic investigations show that NTPZ exhibits a small energy gap, large up-conversion efficiency, low non-radiative decay, and high photoluminescence quantum yield. Further theoretical simulations reveal that the excited molecular vibrations play a key role in regulating the non-radiative decays of the isomers. Therefore, an NTPZ based OLED achieves better electroluminescence performances, such as a higher external quantum efficiency of 27.5% compared to a TNPZ based OLED (18.3%). This isomeric strategy not only provides an opportunity to deeply understand the relationship between substituent locations and molecular properties, but also affords a simple and effective strategy to enrich TADF materials.
More Related Videos
Related Concept Videos
Photoluminescence: Applications
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Photoluminescence: Fluorescence and Phosphorescence
A pair of electrons in a...
Thermal and Photochemical Electrocyclic Reactions: Overview
Variables Affecting Phosphorescence and Fluorescence
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.

