2015
DOI: 10.1016/j.ica.2015.03.037
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A new bifunctional Schiff base as a colorimetric and fluorescence sensor for Al3+ and CN−

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Cited by 31 publications
(7 citation statements)
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“…After report of a commercially available chemosensor (2-hydroxy-1-naphthaldehyde) for Al 3+ ion [24], a few of Schiff-base molecules based on 2-hydroxy-1-naphthaldehyde have been reported for selective detection of the metal ion [25][26][27][28][29][30]. A conjugate of 2-hydroxynaphthaldehyde and 8-aminoquinoline was used for fluorescence sensing of Al 3+ ion [31], spectrofluorimetric determination of different metal ions including Al 3+ and as sensors for Ni 2+ and acetate ions [32].…”
Section: Introductionmentioning
confidence: 99%
“…After report of a commercially available chemosensor (2-hydroxy-1-naphthaldehyde) for Al 3+ ion [24], a few of Schiff-base molecules based on 2-hydroxy-1-naphthaldehyde have been reported for selective detection of the metal ion [25][26][27][28][29][30]. A conjugate of 2-hydroxynaphthaldehyde and 8-aminoquinoline was used for fluorescence sensing of Al 3+ ion [31], spectrofluorimetric determination of different metal ions including Al 3+ and as sensors for Ni 2+ and acetate ions [32].…”
Section: Introductionmentioning
confidence: 99%
“…13 and Table 2). 85 In methanol solution, sensor 16 exhibited weak emission at 550 nm (l ex = 316 nm). Fluorescence titration with Al 3+ revealed a prominent increase in emission intensity accompanied by a blue shift of the emission maxima from 550 nm to 448 nm (Dl shift = 102 nm).…”
Section: Materials Advances Reviewmentioning
confidence: 99%
“…S3, ESI †), which is within the range of those (10 3 -10 9 ) previously reported for Al 3+ binding chemosensors. [74][75][76][77] The detection limit 78 of receptor 1 as a fluorescence sensor for the analysis of Al 3+ ions was found to be 2.01 mM (Fig. S4, ESI †).…”
Section: Fluorescence and Absorption Studies Of 1 Toward Al 3+mentioning
confidence: 99%