Abstract
Fluorescence signals have been widely used in information encryption for a few decades, but still suffer from limited reliability. Here, reversible multichannel fluorescent devices with encrypted information were constructed, based on two fluorescent positional isomers of a diphenylquinoxaline derivative. Possessing the same core fluorescent group and acid-/pH-responsive mechanism, the two isomers showed different fluorescence colors in an acidic environment; this allowed us to realize stepwise encryption of information in orthogonal fluorescence channels. Because the protonation was reversible, the revealed information could be re-encrypted simply by heating. This approach highlights the value of positional isomers to build multichannel encryption devices, improving their reliability on the molecular level.
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CITATION STYLE
Liu, Y., Seeberger, P. H., Merbouh, N., & Loeffler, F. F. (2021). Position Matters: Fluorescent Positional Isomers for Reliable Multichannel Encryption Devices. Chemistry - A European Journal, 27(65), 16098–16102. https://doi.org/10.1002/chem.202103441
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