Issue 8, 2016

Achieving very bright mechanoluminescence from purely organic luminophores with aggregation-induced emission by crystal design

Abstract

Although bright organic mechanoluminescence (ML) has been observed for a few luminophores with aggregation-induced emission (AIE), details of the positive effect of AIE on ML performance remain unclear and a feasible design principle for AIE-ML compounds has not yet been presented. Herein, an effective strategy for the molecular design of efficient AIE-ML materials is demonstrated, based on tetraphenylethene (TPE) building blocks with formyl substituents, which yield non-centrosymmetric crystal structures with prominent piezoelectric properties for molecular excitation combined with AIE features for intense emission. Following this approach, three AIE-active compounds have been developed and are found to show unique ML characteristics. Furthermore, the results of single crystal X-ray analysis and density functional theory (DFT) calculations suggest that the ML performance would probably be further enhanced by creating molecules with larger dipolar moments and enhanced AIE properties.

Graphical abstract: Achieving very bright mechanoluminescence from purely organic luminophores with aggregation-induced emission by crystal design

Supplementary files

Article information

Article type
Edge Article
Submitted
24 Mar 2016
Accepted
23 Apr 2016
First published
26 Apr 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 5307-5312

Achieving very bright mechanoluminescence from purely organic luminophores with aggregation-induced emission by crystal design

B. Xu, W. Li, J. He, S. Wu, Q. Zhu, Z. Yang, Y. Wu, Y. Zhang, C. Jin, P. Lu, Z. Chi, S. Liu, J. Xu and M. R. Bryce, Chem. Sci., 2016, 7, 5307 DOI: 10.1039/C6SC01325B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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