Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1119, Issue -, Pages 151-156Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2016.04.078
Keywords
5-Nitro-1H-indazole; Heterocyclic dyes; Optical properties; Density function theory calculations; Tautomerism
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Funding
- Research Office, Mashhad Branch, Islamic Azad University, Mashhad-Iran
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Tautomerism and alkylation studies on the green intermediate 2-(5-hydroxyimino-1-methyl-4,5-dihydro-1H-4-indazolyliden)-2-phenylacetonitrile led to the synthesis of new heterocyclic green, blue and orange dyes in high yields. The structures of all newly synthesized compounds were confirmed by spectral and analytical data. The optical properties of the dyes were spectrally characterized by using a UV-vis spectrophotometer and results show that they exhibited interesting photophysical properties. Solvent effects on the absorption spectra of these dyes have been studied and the absorption band in polar solvents undergoes a red shift. Density functional theory calculations of the dyes were performed to provide the optimized geometries and relevant frontier orbitals. Calculated electronic absorption spectra were also obtained by time-dependent density functional theory method. (c) 2016 Elsevier B.V. All rights reserved.
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