Litcius/Paper detail

Colorimetric detection of Hg<sup>2+</sup> with an azulene-containing chemodosimeter <i>via</i> dithioacetal hydrolysis

Carlos M. López-Alled, Lloyd C. Murfin, Gabriele Kociok‐Köhn, Tony D. James, Jannis Wenk, Simon E. Lewis

2020The Analyst27 citationsDOIOpen Access PDF

Abstract

Azulene is a bicyclic aromatic chromophore that absorbs in the visible region. Its absorption maximum undergoes a hypsochromic shift if a conjugated electron-withdrawing group is introduced at the C1 position. This fact can be exploited in the design of a colorimetric chemodosimeter that functions by the transformation of a dithioacetal to the corresponding aldehyde upon exposure to Hg2+ ions. This chemodosimeter exhibits good chemoselectivity over other metal cations, and responds with an unambiguous colour change clearly visible to the naked eye. Its synthesis is concise and its ease of use makes it appropriate in resource-constrained environments, for example in determing mercury content of drinking water sources in the developing world.

Topics & Concepts

ChemistryHypsochromic shiftPhotochemistryChromophoreAzuleneBathochromic shiftChemoselectivityAldehydeNaked eyeConjugated systemFluorescenceOrganic chemistryCatalysisChromatographyDetection limitQuantum mechanicsPhysicsPolymerMolecular Sensors and Ion DetectionAdvanced Chemical Sensor TechnologiesMercury impact and mitigation studies
Colorimetric detection of Hg<sup>2+</sup> with an azulene-containing chemodosimeter <i>via</i> dithioacetal hydrolysis | Litcius