[article]
Titre : |
Bisthiocarbohydrazones as colorimetric and “Turn on” fluorescent chemosensors for selective recognition of fluoride |
Type de document : |
texte imprimé |
Auteurs : |
Saravana Loganathan Ashok Kumar, Auteur ; Ramalingam Tamilarasan, Auteur ; Moorthy Saravana Kumar, Auteur |
Année de publication : |
2012 |
Article en page(s) : |
pp. 12379-12383 |
Note générale : |
Chimie industrielle |
Langues : |
Anglais (eng) |
Mots-clés : |
Bisthiocarbohydrazone Heterocyclic |
Résumé : |
Bisthiocarbohydrazone derivatives of two heterocyclic ketones were designed and synthesized to selectively sense fluoride ion from a biologically competing solvent dimethylsulfoxide (DMSO). The selective recognition of fluoride is clearly visible to the naked eye with a distinct color change. The recognition mechanism has been investigated by UV–visible, fluorescence spectroscopy, and 1H NMR titration experiments. From the Benesi–Hidebrand equation and Job's plot, it was inferred that both compounds bind to fluoride with a 1:1 stoichiometry. 1H NMR titration data indicates deprotonation of the NH protons by fluoride as a prominent step in the recognition. |
DEWEY : |
660 |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie2013696 |
in Industrial & engineering chemistry research > Vol. 50 N° 22 (Novembre 2011) . - pp. 12379-12383
[article] Bisthiocarbohydrazones as colorimetric and “Turn on” fluorescent chemosensors for selective recognition of fluoride [texte imprimé] / Saravana Loganathan Ashok Kumar, Auteur ; Ramalingam Tamilarasan, Auteur ; Moorthy Saravana Kumar, Auteur . - 2012 . - pp. 12379-12383. Chimie industrielle Langues : Anglais ( eng) in Industrial & engineering chemistry research > Vol. 50 N° 22 (Novembre 2011) . - pp. 12379-12383
Mots-clés : |
Bisthiocarbohydrazone Heterocyclic |
Résumé : |
Bisthiocarbohydrazone derivatives of two heterocyclic ketones were designed and synthesized to selectively sense fluoride ion from a biologically competing solvent dimethylsulfoxide (DMSO). The selective recognition of fluoride is clearly visible to the naked eye with a distinct color change. The recognition mechanism has been investigated by UV–visible, fluorescence spectroscopy, and 1H NMR titration experiments. From the Benesi–Hidebrand equation and Job's plot, it was inferred that both compounds bind to fluoride with a 1:1 stoichiometry. 1H NMR titration data indicates deprotonation of the NH protons by fluoride as a prominent step in the recognition. |
DEWEY : |
660 |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie2013696 |
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