Loading…
Sensitizing the phosphorescence of pyromellitic diimide through non-covalent halogen-carbonyl interactions
In this study, we efficiently sensitize pyromellitic diimide's triplets by cocrystallizing with heavy bromine-substituted small aromatics. The resulting halogen bonding interactions mediate an external heavy atom effect, leading to remarkable ambient phosphorescence with one of the highest quan...
Saved in:
Published in: | CrystEngComm 2024-09, Vol.26 (37), p.5129-5132 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | In this study, we efficiently sensitize pyromellitic diimide's triplets by cocrystallizing with heavy bromine-substituted small aromatics. The resulting halogen bonding interactions mediate an external heavy atom effect, leading to remarkable ambient phosphorescence with one of the highest quantum yields reported to date.
Herein, a halogen-bonding-assisted heavy-atom effect was introduced to sensitize the locally-excited triplet state of pyromellitic diimide, achieving efficient phosphorescence, with one of the highest quantum yield in a cocrystal. |
---|---|
ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d4ce00812j |