2015
DOI: 10.1039/c5cc01280e
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A reversible and selective chemosensor based on intramolecular NH⋯NH2 hydrogen bonding for cyanide and pH detection

Abstract: A highly selective and reversible chemosensor for cyanide and pH detection was developed based on intramolecular NH···NH2 hydrogen bonding.

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Cited by 46 publications
(12 citation statements)
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“…12 Currently, fluorescent probes for the detection of cyanide anions take advantage of their characteristic properties such as strong nucleophilicity and high affinity towards copper ions. Cyanide sensors are based on hydrogen bonding, 13,14 nucleophilic addition to the carbonyl moiety, [15][16][17] and formation of cyanide anion complexes. [18][19][20] Among these reactions, the nucleophilic addition was found to have a high selectivity and sensitivity for the recognition of cyanide anions.…”
Section: Introductionmentioning
confidence: 99%
“…12 Currently, fluorescent probes for the detection of cyanide anions take advantage of their characteristic properties such as strong nucleophilicity and high affinity towards copper ions. Cyanide sensors are based on hydrogen bonding, 13,14 nucleophilic addition to the carbonyl moiety, [15][16][17] and formation of cyanide anion complexes. [18][19][20] Among these reactions, the nucleophilic addition was found to have a high selectivity and sensitivity for the recognition of cyanide anions.…”
Section: Introductionmentioning
confidence: 99%
“…We wondered whether dosimeter 7 would also work in the solid state . The probe was adsorbed onto filter papers by immersing a filter paper in a DCM solution of dosimeter 7 (0.5 mmol/L) for 20 min and then drying it in air.…”
Section: Resultsmentioning
confidence: 99%
“…The design of colorimetric probes based on the signal unit ( uorophore or chromophore) with binding sites (usually employed NH or OH) to detect cyanide have been widely studied due to its relative acidity of NH or OH group, which can form hydrogen bonding with cyanide or induce deprotonation favoring the uorescent and colorimetric changes [18][19][20][21]. Recently, the activated CH group, such as the CHCN group, was successfully employed as a binding site to develop a series of cyanide probes [22][23][24][25][26]. Especially, similar naphthalimide uorophore containing different binding sites, such as 1a (NH) [27], 1b (OH) [28] and 1c (CHCN) [29], have different redshift wavelengths of probes with uoride.…”
Section: Introductionmentioning
confidence: 99%