2010
DOI: 10.1021/ol101281x
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Specific Recognition and Sensing of CN in Sodium Cyanide Solution

Abstract: Specific recognition of CN(-) in sodium cyanide solution was achieved using two imidazole-based receptors (A and B). Visually detectable color changes were associated with the formation of hydrogen bonded adducts, A.CN(-) and B.CN(-). Ratiometric fluorescence response was achieved for receptor A on binding to CN(-), and this reagent was used for imaging bacterial cells pre-exposed to 1.42 microM CN(-) solution.

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Cited by 209 publications
(77 citation statements)
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“…124) were used for the chromo-fluorogenic sensing of anion CN -. 165 Regarding the chromogenic response, the CH 3 CN:water (HEPES buffer) Ferrocene-fused imidazole dyads 256 and 257 (see Fig. 126 Carbazolo[1,2-a]carbazole receptor 259 (see Fig.…”
Section: 11-containing Polycyclic Aromatic Hydrocarbonsmentioning
confidence: 99%
“…124) were used for the chromo-fluorogenic sensing of anion CN -. 165 Regarding the chromogenic response, the CH 3 CN:water (HEPES buffer) Ferrocene-fused imidazole dyads 256 and 257 (see Fig. 126 Carbazolo[1,2-a]carbazole receptor 259 (see Fig.…”
Section: 11-containing Polycyclic Aromatic Hydrocarbonsmentioning
confidence: 99%
“…Whereas, other anions including F  and AcO  ions fails to show sensitivity towards R1-R4 in 25% aqueous DMSO. Higher basicity (or nucleophilicity) as well as the lower hydration energy values [36] of cyanide ion (ΔH hyd = -67 kJ/mol) play a major role in selective detection of CN  ion over fluoride (ΔH hyd = -505 kJ/mol) and acetate (∆H hyd = -375 kJ/mol) ions. Thus, the much lower hydration energy of CN  ions preferably and selectively interact with R1-R4 in 25% organo-aqueous mixed solvent medium.…”
Section: Colorimetric Titrationmentioning
confidence: 99%
“…[187]. Various derivatives of 2-phenyl-1H-anthra[1,2-d]imidazole-6,11-dione (20) were also prepared using methyl and hydroxy substituted benzaldehyde (13) in presence of sodium acetate in acetic acid under refluxing condition (Scheme 12) [188].…”
Section: Synthesis Of 2-arylbenzimidazoles From O-phenylenediamines Amentioning
confidence: 99%