2016
DOI: 10.1016/j.talanta.2016.08.061
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Simultaneous bioimaging recognition of Al3+ and Cu2+ in living-cell, and further detection of F− and S2− by a simple fluorogenic benzimidazole-based chemosensor

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Cited by 85 publications
(19 citation statements)
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“…Various metal ions [51,52] were selected to study their sensitivity to HFNs and the results are shown in Figure 6f. We found that the intensity of HFNs is very sensitive to Cu(II) compared with the other metal ions, which is also reported elsewhere [53][54][55]. The fluorescence selectivity was investigated to understand the behavior of HFNs and HFNs dispersed in different cation Ag(I), Cd(II), Cu(II), Ca(II), Cr(III), Mg(II), Ni(II) and Pb(II) solutions.…”
Section: Fluorescence-based Detection Of Cu(ii) Ionssupporting
confidence: 78%
“…Various metal ions [51,52] were selected to study their sensitivity to HFNs and the results are shown in Figure 6f. We found that the intensity of HFNs is very sensitive to Cu(II) compared with the other metal ions, which is also reported elsewhere [53][54][55]. The fluorescence selectivity was investigated to understand the behavior of HFNs and HFNs dispersed in different cation Ag(I), Cd(II), Cu(II), Ca(II), Cr(III), Mg(II), Ni(II) and Pb(II) solutions.…”
Section: Fluorescence-based Detection Of Cu(ii) Ionssupporting
confidence: 78%
“…In recent times, a paradigm drift towards the development of simple molecule based multifunctional chemosensors, potentially capable to selectively target both metal ions as well as small molecules of environmental and biological significance, is witnessed in the field of analytical research. [1,2] These multiple target sensors have many advantages over single ion recognition based traditional chemosensors such as easy synthetic protocols, cost effectiveness, superb efficiency towards multiple targets of interest, easy sample preparation, real time responses, operational simplicity and recoverability. [3][4][5][6][7] Azine based Schiff base molecular systems, which are recognized with easy synthetic protocols, provide ample opportunities to develop push-pull architectures with D-π-A type conjugation through azine linkages in conjunction with excellent chromophoric units.…”
Section: Introductionmentioning
confidence: 99%
“…For instance, anthracene, 10,11 anthraquinone, 12,13 calixpyrrole, 14,15 dipyrrolylquinoxaline, 16 and other chromophore molecules have been used as chromogenic units, displaying various colors and/or uorescence. In addition, uoride-binding motifs such as urea, 17,18 thiourea, 19,20 hydrazide, 21,22 indole, 23,24 and imidazole 23,25 groups have been adopted for selective recognition of uoride. The receptor groups mostly recognize uoride by Hbonding or deprotonation of the -NH moiety.…”
Section: Introductionmentioning
confidence: 99%