2006
DOI: 10.1016/j.tetlet.2006.09.035
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Colorimetric and fluorescence sensing of anions using thiourea based coumarin receptors

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Cited by 93 publications
(29 citation statements)
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“…Although the determination of fluorescence quenching is able to give important knowledge on the photophysical processes occurring in the formation of coumarin complexes, few fluorescence quenching studies have been performed on the coumarins until now, most of them concerning only organic quenchers, and none the lanthanides [26][27][28][29][30][31].…”
Section: Introductionmentioning
confidence: 99%
“…Although the determination of fluorescence quenching is able to give important knowledge on the photophysical processes occurring in the formation of coumarin complexes, few fluorescence quenching studies have been performed on the coumarins until now, most of them concerning only organic quenchers, and none the lanthanides [26][27][28][29][30][31].…”
Section: Introductionmentioning
confidence: 99%
“…[29,30] Gunnlaugsson and co-workers have developed similar chemosensors for anions by using anthracene-based fluorescent sensors. [20,31,32] Other examples of recently synthesised thiourea sensors include hosts with the thiourea group linked to fluorescent sensor moieties by a rigid hydrazine spacer selective for acetate, [33][34][35][36] Hosts based on coumarin sensors that act as both fluorescent and colorimetric sensors [37] and compounds that utilise cooperativity between the thiourea group and an amine group adjacent to a naphthalimide sensor are also known. [38,39] Sensors using 2 + (4) binds anions in both 1:1 and 1:2 species, whereas the free ligand is ineffective because of intramolecular NH···N hydrogen bonding.…”
Section: Introductionmentioning
confidence: 99%
“…Upon interaction with H 2 PO 4 − , the reduction potential of compound 2 was enhanced, namely the electron transfer from the electron rich phenol moiety bonded with H 2 PO 4 − to the electron deficient -NO 2 moiety became more feasible. Upon further addition of H 2 PO 4 − , it appeared that the deprotonated species LH − , being more electron rich compared to the hydrogenbonded complex with H 2 PO 4 − , activated the ICT process more efficiently 23 . Compared with compound 1, the different interacted mechanism was induced by the different site which the nitro group existed.…”
Section: Fluorescence Titrationmentioning
confidence: 99%