Synthesis of benzimidazoles containing pyrazole group and quantum chemistry calculation of their spectroscopic properties and electronic structure.
J Fluoresc
; 22(1): 201-12, 2012 Jan.
Article
em En
| MEDLINE
| ID: mdl-21826423
ABSTRACT
Five benzimidazole compounds containing pyrazole group were synthesized via one-step reaction of o-phenylenediamine and 1-arylpyrazole-4-carbaldehyde in ethanol under mild conditions. The composition and structure of resultant benzimidazole compounds were analyzed by means of elemental analysis, mass spectrometry, (1)H-nuclear magnetic resonance spectroscopy and X-ray single crystal diffraction. The ultraviolet-visible light spectra and fluorescent spectra of the products were measured. Their ground-state (S(0)) equilibrium geometries and vibrational frequencies were determined based on B3LYP method, and their first excited-state (S(1)) geometries were fully optimized based on 6-31G (d, p) basis set of TD-B3LYP method. Besides, the spectroscopic properties of the products were computed based on cc-pVTZ basis set of TD-B3LYP method and compared with corresponding experimental data. It has been found that benzimidazole compounds containing pyrazole group can be readily synthesized in a high yield via one-step reaction of o-phenylenediamine and 1-arylpyrazole-4-carbaldehyde in ethanol solvent. The fluorescence properties of the five synthesized compounds are closely related to their molecular structure; and their computed fluorescence spectra well correspond to their experimental values. Moreover, they have stable structure and strong fluorescence, showing potential application in time-resolved fluoroimmunoassay and DNA probe.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Pirazóis
/
Teoria Quântica
/
Análise Espectral
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Benzimidazóis
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Elétrons
Idioma:
En
Revista:
J Fluoresc
Ano de publicação:
2012
Tipo de documento:
Article