Issue 12, 2022

Ultralong blue room-temperature phosphorescence by cycloalkyl engineering

Abstract

The development of organic room-temperature phosphorescence (RTP) materials with ultralong lifetimes is desired but remains challenging, especially those with blue RTP emission. Herein, through the cycloalkyl modification of a phenothiazine-5,5-dioxide (CsO) core, ultralong blue RTP performance with a lifetime up to 1116.10 ms has been achieved by C6-CsO with cyclohexyl (C6) as the substituent, which is about 1500 times that of the similar compound N6-CsO with hexyl (N6) as the side chain, indicating the superiority of cycloalkyl to the commonly used alkyl engineering. The crystal structure and DFT calculations revealed that the smaller steric hindrance of the cycloalkyl moieties than those of alkyl ones, together with the increased intermolecular interactions, contributing to the optimized RTP property. It provides a universal way to develop ultralong blue RTP materials, which can promote their practical applications by deeply understanding of inherent mechanism.

Graphical abstract: Ultralong blue room-temperature phosphorescence by cycloalkyl engineering

Supplementary files

Article information

Article type
Research Article
Submitted
31 မတ် 2022
Accepted
05 မေ 2022
First published
06 မေ 2022

Mater. Chem. Front., 2022,6, 1606-1614

Ultralong blue room-temperature phosphorescence by cycloalkyl engineering

Z. Cong, M. Han, Y. Fan, Y. Fan, K. Chang, L. Xiao, Y. Zhang, X. Zhen, Q. Li and Z. Li, Mater. Chem. Front., 2022, 6, 1606 DOI: 10.1039/D2QM00284A

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