Issue 37, 2024

Sensitizing the phosphorescence of pyromellitic diimide through non-covalent halogen–carbonyl interactions

Abstract

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.

Graphical abstract: Sensitizing the phosphorescence of pyromellitic diimide through non-covalent halogen–carbonyl interactions

Supplementary files

Article information

Article type
Communication
Submitted
15 Aug 2024
Accepted
29 Aug 2024
First published
06 Sep 2024

CrystEngComm, 2024,26, 5129-5132

Sensitizing the phosphorescence of pyromellitic diimide through non-covalent halogen–carbonyl interactions

D. Hati, S. Garain, S. N. Ansari, A. A. Kongasseri and S. J. George, CrystEngComm, 2024, 26, 5129 DOI: 10.1039/D4CE00812J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements