Abstract

AbstractAzulene derivatives that have an azathiacrown ether moiety were synthesized by using a modification of the method described by Vögtle and co‐workers. These compounds are highly selective for detecting Ag+ions, which is demonstrated visually by a color change from orange to violet. Structural studies of the Ag+‐induced colored product by NMR spectroscopy and ESI‐MS identified a 1:1 (Ag+:ligand) complex formed by the coordination of Ag+ion with the azathiacrown ether moiety. Competition experiments in the presence of other metal ions, ESI MS/MS experiments on the Ag+and Hg2+complexes, and DFT calculations on the Ag+complex suggest that the high selectivity and color change for Ag+ion is due to the relatively strong binding of the azathiacrown ether moiety to Ag+ion, and not to π–cation interactions. Azulene derivatives that are highly selective toward a particular heavy metal ion and undergo a distinct color change have not been reported before.

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