Highly sensitive and selective fluorescent sensor for zinc ion based on a new diarylethene with a thiocarbamide unit

The Journal of Physical Chemistry. B
Congcong ZhangGang Liu

Abstract

A new photochromic diarylethene has been synthesized by using thiocarbamide as a functional group and perfluordiarylethene as photoswitching trigger via a salicylidene Schiff base linkage. The diarylethene could be used as a multicontrollable fluorescence switch when triggered by base/acid, light, and metal ions. The results showed that the absorption and fluorescence characteristics of the diarylethene exhibited sequence-dependent responses through efficient interaction of specific salicylidene Schiff base-linked thiocarbamide unit with tetrabutylammonium hydroxide/trifluoroacetic acid and photoirradiation. Moreover, the diarylethene was highly selective toward Zn(2+) ion with obvious fluorescence change from light blue to bright yellow in acetonitrile. The deprotonated form of the diarylethene had typical photochromism, but it showed an irreversible photocyclization reaction after binding with Zn(2+). Finally, two logic circuits were constructed by using the fluorescence intensity as the output signal with the inputs of the combinational stimuli of light and chemical species.

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Citations

Jun 8, 2017·Luminescence : the Journal of Biological and Chemical Luminescence·Lili LiShouzhi Pu
Jul 1, 2017·Dalton Transactions : an International Journal of Inorganic Chemistry·Tânia V PintoCristina Freire
Nov 23, 2016·Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology·X G TangS Z Pu

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