Highly selective sensing of cyanide by a benzochromene-based ratiometric fluorescence probe
摘要:
Enone-functionalized benzochromene chemodosimeter (1) was prepared through the Baylis-Hillman condensation reaction and was utilized as a ratiometric fluorescence probe for cyanide anions in aqueous buffer. The probe has shown a selective and sensitive response to cyanides over other various anions through the Michael addition and a subsequent [1,3]-sigmatropic rearrangement reaction. When cyanide anions were added, a prominent ratiometric fluorescence change of 1 was observed thus allowing to detect the micromolar concentration of cyanides by the naked eye. (C) 2012 Elsevier Ltd. All rights reserved.
A convenient general synthesis of 3-substituted 2H-chromene derivatives
作者:Perry T Kaye、Xolani W. Nocanda
DOI:10.1039/b201827f
日期:2002.5.10
Reactions of 2-hydroxybenzaldehydes and 2-hydroxy-1-naphthaldehydes with various activated alkenes under Baylis–Hillman conditions have been shown to proceed with regioselective cyclisation to afford the corresponding 3-substituted chromene derivatives. In some cases competitive dimerisation of the alkene component was observed, and direct dimerisation in the absence of the aldehyde has been explored.
Highly selective sensing of cyanide by a benzochromene-based ratiometric fluorescence probe
作者:Heejin Lee、Hae-Jo Kim
DOI:10.1016/j.tetlet.2012.07.128
日期:2012.10
Enone-functionalized benzochromene chemodosimeter (1) was prepared through the Baylis-Hillman condensation reaction and was utilized as a ratiometric fluorescence probe for cyanide anions in aqueous buffer. The probe has shown a selective and sensitive response to cyanides over other various anions through the Michael addition and a subsequent [1,3]-sigmatropic rearrangement reaction. When cyanide anions were added, a prominent ratiometric fluorescence change of 1 was observed thus allowing to detect the micromolar concentration of cyanides by the naked eye. (C) 2012 Elsevier Ltd. All rights reserved.