2015
DOI: 10.1039/c5ra08086j
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Exploitation of a new Schiff-base ligand for boric acid fluorescent sensing in aqueous medium with bio-imaging studies in a living plant system

Abstract: Graphical AbstractA new Schiff-base ligand owing to 1:1 chelation with boric acid exhibits selective boric acid fluorosensor at physiological condition along with bio-imaging facilities. B(OH) 3 h  F~ 0.007 Weak Emission ESPTA hydrolysis resistant Schiff-base ligand (L1) consisting of aromatic aldimine moiety appended to a triazole precursor along with phenolic-OH has been synthesized which acts as a fluorescence probe and exhibits rare selective sensing ability for Boric Acid (BA) in aqueous buffer medium a… Show more

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Cited by 7 publications
(1 citation statement)
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“…37 The detailed synthetic procedures for the Schiff-base molecule, 2-((4H-1,2,4-triazol-4-ylimino)methyl)-6-(hydroxymethyl)-4methylphenol (AH), are mentioned elsewhere. 38 In brief, 4-amino-4H-1,2,4-triazole (Tz) (0.084 g, 1 mmol) was added drop-wise to a methanolic solution of HHMB (0.166 g, 1 mmol) by constant stirring, and 2 drops of acetic acid were further added to the solution. The mixture was refluxed for 2 h and subsequently filtered.…”
Section: Synthesis Of a Schiff-base Moleculementioning
confidence: 99%
“…37 The detailed synthetic procedures for the Schiff-base molecule, 2-((4H-1,2,4-triazol-4-ylimino)methyl)-6-(hydroxymethyl)-4methylphenol (AH), are mentioned elsewhere. 38 In brief, 4-amino-4H-1,2,4-triazole (Tz) (0.084 g, 1 mmol) was added drop-wise to a methanolic solution of HHMB (0.166 g, 1 mmol) by constant stirring, and 2 drops of acetic acid were further added to the solution. The mixture was refluxed for 2 h and subsequently filtered.…”
Section: Synthesis Of a Schiff-base Moleculementioning
confidence: 99%