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Isatin-1,8-Naphthalimide Hydrazones: A Study of Their Sensor and ON/OFF Functionality
Five novel hydrazones derived from substituted isatins were synthesized as potential anion sensors. Using UV-VIS, FTIR, NMR and fluorescence spectroscopy, these compounds’ tautomeric equilibrium and Z-E photoisomerization were studied in DMF and CHCl(3), depending on the hydrazone concentrations, th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385022/ https://www.ncbi.nlm.nih.gov/pubmed/30678292 http://dx.doi.org/10.3390/molecules24030397 |
Sumario: | Five novel hydrazones derived from substituted isatins were synthesized as potential anion sensors. Using UV-VIS, FTIR, NMR and fluorescence spectroscopy, these compounds’ tautomeric equilibrium and Z-E photoisomerization were studied in DMF and CHCl(3), depending on the hydrazone concentrations, the presence of basic anions and light stimulation. Anion recognition aspects (PF(6)(−), HSO(4)(−), Br(−), Cl(−), NO(3)(−), F(−) and CH(3)COO(−)) and these receptors’ detection limits were also studied. We also tested the light-stimulated ON-OFF functionality of these compounds in the presence or absence of these anions. |
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