Issue 9, 2019

Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence

Abstract

A pair of chiral aggregation-induced emission (AIE) enantiomers and their racemate exhibit not only distinctively different circularly polarized luminescence behaviors, but also completely opposite mechanoluminescence (ML) activities. The data from single crystal analysis identifies that the bright ML of the AIE enantiomers is probably activated by their molecular chirality, which enables unique chiral crystal structures with a polar space group and compact molecular packing. These experimental findings provide a direction for harvesting prominent ML from AIE luminogens. Concurrently, high contrast mechanochromism with larger ΔλPL,max and ΔΦF,s values by up to 140 nm and 0.61 respectively have been achieved from this AIE system, which represents the state-of-the-art mechanochromic performance for ML emitters. Moreover, force-induced white-light emission and thermally activated delayed fluorescence have also been observed. The results of theoretical calculations suggest that the destruction of intermolecular interactions and conversion of molecular conformation account for the significant multiple-variations in emission properties triggered by a single mechanical stimulus.

Graphical abstract: Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence

Supplementary files

Article information

Article type
Research Article
Submitted
15 May 2019
Accepted
19 Jun 2019
First published
20 Jun 2019

Mater. Chem. Front., 2019,3, 1800-1806

Chirality-activated mechanoluminescence from aggregation-induced emission enantiomers with high contrast mechanochromism and force-induced delayed fluorescence

Y. Chen, C. Xu, B. Xu, Z. Mao, J. Li, Z. Yang, N. R. Peethani, C. Liu, G. Shi, F. L. Gu, Y. Zhang and Z. Chi, Mater. Chem. Front., 2019, 3, 1800 DOI: 10.1039/C9QM00312F

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