| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1230932 | Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2013 | 10 Pages |
In this paper we investigate the relationship between molecular structure of alkali metal vanillate molecules and their antimicrobial activity. To this end FT-IR, FT-Raman, UV absorption and 1H, 13C NMR spectra for lithium, sodium, potassium, rubidium and caesium vanillates in solid state were registered, assigned and analyzed. Microbial activity of studied compounds was tested against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Proteus vulgaris, Bacillus subtilis and Candida albicans. In order to evaluate the dependence between chemical structure and biological activity of alkali metal vanillates the statistical analysis was performed for selected wavenumbers from FT-IR spectra and parameters describing microbial activity of vanillates. The geometrical structures of the compounds studied were optimized and the structural characteristics were determined by density functional theory (DFT) using at B3LYP method with 6-311++G** as basis set. The obtained statistical equations show the existence of correlation between molecular structure of vanillates and their biological properties.
Graphical abstractThe degree of growth inhibition exhibited by studied compounds in relation to Escherichia coli (EC), Proteus vulgaris (PV), Pseudomonas aeruginosa (PA), Bacillus subtilis (BS), Staphylococcus aureus (SA) and Candida albicans (CA) evaluated by means of turbidimetry method by measuring optical density of water solutions at 600 nm after 48 h incubation.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► In this work we studied the relationship between molecular structure and biological activity of vanillic acid and alkali metal vanillates. ► To this end FT-IR, FT-Raman, UV absorption and 1H, 13C NMR spectra for lithium, sodium, potassium, rubidium and caesium vanillates in solid state were registered, assigned and analyzed. ► Microbial activity of studied compounds was tested against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Proteus vulgaris, Bacillus subtilis and Candida albicans.
