20248-87-7Relevant articles and documents
Colorimetric Cyanide Chemosensor Based on 1′,3,3′,4-Tetrahydrospiro[chromene-2,2′-indole]
Dagiliene, Migle,Martynaitis, Vytas,Kri??iuˉniene, Vilija,Krik?tolaityte, Sonata,?a?kus, Algirdas
, p. 363 - 369 (2015/06/30)
A new class of chemosensors based on the 1′,3,3′,4-tetrahydrospiro[chromene-2,2′-indole] ring system, which detects cyanide with high specificity, is described. These chemosensors show a distinct color change when treated with cyanide in acetonitrile solution buffered with sodium phosphate, and this procedure is not affected by the presence of other common anions. The chemisensors exhibit high sensitivity to low concentrations of cyanide, meeting the European Union water quality control criterion of sensitivity below 0.05 mg L-1, and show a very fast response within tens of seconds. The mechanism for detection is rationalized by the nucleophilic substitution of the phenolic oxygen atom at the indoline C-2 atom by the cyanide anion to form a stable indolylnitrile adduct and to generate the colored 4-nitrophenolate chromophore. These chemosensors can be synthesized by a simple procedure from commercially available starting materials.
Spectroscopic detection of diols and sugars by acolour change in boronic acid-appended spirobenzopyrans
Shinmori, Hideyuki,Takeuchi, Masayuki,Shinkai, Seiji
, p. 1 - 4 (2007/10/03)
Boronic acid-appended spiropyrans have been synthesized in order to detect diols and sugars by a colour change: only when the boron atom could intramolecularly interact with the tertiary amine in the spiropyran moiety, did added diols and sugars change the shift of the spiropyran-merocyanine equilibrium, which was visually detectable as a colour change.
