2017
DOI: 10.1039/c6nj03794a
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Turn-on fluorescent sensor for the detection of cyanide based on a novel dicyanovinyl phenylacetylene

Abstract: A novel phenylacetylene derivative (3) was successfully synthesized via Sonogashira coupling and a Knoevenagel reaction for cyanide ion detection.

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Cited by 43 publications
(15 citation statements)
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“…4). 33 There was a fluorescence enhancement upon the addition of cyanide. Probe 6 showed an emission band at 460 nm in ACN/H 2 O solution (9 : 1 v/v, 10 mM PBS buffer pH = 10.0) with excitation at 368 nm.…”
Section: Fluorescent Probes Based On a Triphenylamine Platform For An...mentioning
confidence: 99%
“…4). 33 There was a fluorescence enhancement upon the addition of cyanide. Probe 6 showed an emission band at 460 nm in ACN/H 2 O solution (9 : 1 v/v, 10 mM PBS buffer pH = 10.0) with excitation at 368 nm.…”
Section: Fluorescent Probes Based On a Triphenylamine Platform For An...mentioning
confidence: 99%
“…It is likely that the dicyanovinyl groups prohibit the fluorescence emission of their excited states. [26][27][28][29] Figure 2 UV-Vis spectra of P1 and P2 (10 µM) in 100% DMSO…”
Section: Synlettmentioning
confidence: 99%
“…The results conrmed the selective detection of CN À based on nucleophilic addition of CN À ion in the pconjugated position of dicyanovinyl moiety. 16,[54][55][56][57][58][59][60][61][62] In addition, the structure and the binding mechanism were further analysed by FT-IR analysis of free BBCN and BBCN-CN À (Fig. S10 †).…”
Section: Sensing Mechanismmentioning
confidence: 99%