Issue 4, 2013

Tunable solid-state photoluminescence based on proton-triggered structural transformation of 4,4′-bipyridinium derivative

Abstract

An organic molecular system with proton-tunable photoluminescence properties based on a mono-substituted bipyridinium derivative 1-(3-carboxybenzyl)-4,4′-bipyridinium chloride, which possesses both pyridine and carboxylic acid groups as proton-responsive units, has been developed. Through controlling the pH value of the self-assembled systems, three compounds with different degrees of protonation have been obtained. These compounds display distinctly different luminescence behaviors and undergo solid-state structural conversion in response to changes in pH values. In particular, luminescence switching triggered by acid–base vapor can be realized.

Graphical abstract: Tunable solid-state photoluminescence based on proton-triggered structural transformation of 4,4′-bipyridinium derivative

Supplementary files

Article information

Article type
Paper
Submitted
04 Sep 2012
Accepted
07 Nov 2012
First published
07 Nov 2012

J. Mater. Chem. C, 2013,1, 744-750

Tunable solid-state photoluminescence based on proton-triggered structural transformation of 4,4′-bipyridinium derivative

X. Zhou, C. Chen, C. Ren, J. Sun and J. Zhang, J. Mater. Chem. C, 2013, 1, 744 DOI: 10.1039/C2TC00111J

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