Issue 31, 2013

Multi-addressable molecular switches based on a new diarylethene salicylal Schiff base derivative

Abstract

A novel photochromic diarylethene with a salicylidene Schiff base substituent has been synthesized and characterized. The diarylethene could be used as a multi-addressable fluorescence switch when triggered by light, protons and metal ions. As a result, two logic circuits were constructed with the unimolecular platform by using the fluorescence intensity at different wavelengths as outputs and appropriate combinational stimuli of UV/Vis light, TEA/TFA, and Al(III)/EDTA as inputs. Moreover, the diarylethene derivative was found to be highly selective towards Al(III) with significant color and fluorescence changes for potential applications as colorimetric fluorescent chemosensors.

Graphical abstract: Multi-addressable molecular switches based on a new diarylethene salicylal Schiff base derivative

Supplementary files

Article information

Article type
Paper
Submitted
29 Apr 2013
Accepted
31 May 2013
First published
03 Jun 2013

J. Mater. Chem. C, 2013,1, 4726-4739

Multi-addressable molecular switches based on a new diarylethene salicylal Schiff base derivative

S. Pu, Z. Tong, G. Liu and R. Wang, J. Mater. Chem. C, 2013, 1, 4726 DOI: 10.1039/C3TC30804A

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