2021
DOI: 10.1002/slct.202103730
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A Schiff‐Base Molecular Keypad LockandTurn‐On Sensor for Selective Detection of Fe3+ with INHIBIT Logic Behaviour

Abstract: A novel emissive Schiff-base (3)has been synthesized through single-step condensation of sulfanilamide and fluorogenic 3formylchromone. Compound (3) senses Fe 3 + ion in semiaqueous media. Both fluorogenic and colorimetrical changes were observed in the presence of Fe 3 + ions. Interestingly, on introduction of EDTA into the putative complex, [(3) + Fe 3 + ], the spectroscopic changes were reversed. The ligand detects Fe 3 + ions sensitively as the limit of detection for Fe 3 + ion was 9.3 × 10 À 7 M. The prob… Show more

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Cited by 4 publications
(2 citation statements)
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“…Chromones are naturally occurring compounds which are widely known to have anticancer, antioxidant and other biological properties [1] . Chromone derivatives with Schiff base groups have been studied due to properties to form complexes with metal ions such as copper (II), platinum (II), nickel (II) and other transition metals, [1–6] including chromone‐based sensors for the detection of anions [7] . The development of colorimetric sensors for the detection of environmentally and biologically important ionic species is currently of great interest [8–11] .…”
Section: Introductionmentioning
confidence: 99%
“…Chromones are naturally occurring compounds which are widely known to have anticancer, antioxidant and other biological properties [1] . Chromone derivatives with Schiff base groups have been studied due to properties to form complexes with metal ions such as copper (II), platinum (II), nickel (II) and other transition metals, [1–6] including chromone‐based sensors for the detection of anions [7] . The development of colorimetric sensors for the detection of environmentally and biologically important ionic species is currently of great interest [8–11] .…”
Section: Introductionmentioning
confidence: 99%
“…To this homogenous solution 50.00 μl of glacial AcOH was added drop‐wise and the reaction mixture was allowed to stir along with constant heating at 50 °C until the reaction completion (TLC, 5 h) (Scheme 1). [34] The precipitates obtained after overnight stirring were collected and washed with ether (2×25.00 ml) and recrystallized from methanol to obtain final product, 4‐((3‐nitrobenzylidene)amino)benzene sulfonamide (3) .…”
Section: Resultsmentioning
confidence: 99%