Issue 38, 2018

Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

Abstract

A new levorotatory compound ((S)-9,9′-(6-(1-phenylethoxy)-1,3,5-triazine-2,4-diyl)bis(9H-carbazole)) and its corresponding racemic compound show different intermolecular interactions to restrain nonradiative transition, resulting in an enhanced ultralong organic phosphorescence lifetime from 229.0 ms to 419.8 ms. This work will provide a new insight into the chirality of organic molecules to adjust the ultralong phosphorescence.

Graphical abstract: Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

Supplementary files

Article information

Article type
Communication
Submitted
05 liep. 2018
Accepted
02 rugs. 2018
First published
03 rugs. 2018

J. Mater. Chem. C, 2018,6, 10179-10183

Insight into chirality on molecular stacking for tunable ultralong organic phosphorescence

C. Ma, H. Ma, K. Ling, R. Zheng, M. Gu, L. Song, Z. An, H. Shi and W. Huang, J. Mater. Chem. C, 2018, 6, 10179 DOI: 10.1039/C8TC03297A

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