6533b851fe1ef96bd12a8d51

RESEARCH PRODUCT

A dual channel sulphur-containing a macrocycle functionalised BODIPY probe for the detection of Hg(II) in a mixed aqueous solution

José V. Ros-lisMaria Lo PrestiSusana P. G. CostaFélix SancenónRosa Maria Ferreira BatistaRamón Martínez-máñezM. Manuela M. Raposo

subject

:Ciências Químicas [Ciências Naturais]BodipyHeterocyclesColorimetric sensor010402 general chemistryPhotochemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundSynthesisQUIMICA ORGANICABODIPYMaterials ChemistryFluorimetric sensorDetection in aqueous solutionAcetonitrileDual channel chemosensorCrown etherchemistry.chemical_classificationAqueous solutionScience & Technology010405 organic chemistryChemistryOptical chemosensorQUIMICA INORGANICAWaterGeneral ChemistryMercuryCiências Naturais::Ciências QuímicasFluorescence3. Good health0104 chemical sciencesAbsorption bandvisual_artHg (II)Coordinationvisual_art.visual_art_mediumHypsochromic shiftfluorescenceBODIPYCrown ether

description

We report herein the synthesis and chromo-fluorogenic behaviour of a new probe 1 containing a boron-dipirromethene (BODIPY) unit electronically connected with a dithia-dioxa-aza macrocycle. Acetonitrile and water-acetonitrile 95:5 v/v solutions of the probe showed an ICT band in the visible zone and are nearly non-emissive. When acetonitrile was used as solvent, addition of Hg(II) and trivalent metal cations induced an hypsochromic shift of the absorption band and moderate emission enhancements. A highly selective response was obtained when using competitive media such as wateracetonitrile 95:5 v/v. In this case only Hg(II) induced a hypsochromic shift of the absorption band and a marked emission enhancement.

10.13039/501100003359https://dx.doi.org/10.1039/c7nj04699e