4.7 Article

Looking for Minor Phenolic Compounds in Extra Virgin Olive Oils Using Neutron and Raman Spectroscopies

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ANTIOXIDANTS
卷 10, 期 5, 页码 -

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MDPI
DOI: 10.3390/antiox10050643

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extra virgin olive oil; minor polar compounds; inelastic neutron scattering; Raman spectroscopy; UV-Vis spectroscopy

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  1. NAST Centre, Universita degli Studi di Roma Tor Vergata

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The vibrational spectroscopic signals of EVOO samples were fully characterized using Inelastic Neutron Scattering (INS) and Raman spectroscopies. The spectra were dominated by CH2 vibrations, especially at around 750 cm(-1) and 1300 cm(-1). The structure-activity information related to minor polar compounds can be found in specific spectral regions, such as 675 and 1200 cm(-1) for hydroxytyrosol, and around 450 cm(-1) for all minor polar compounds used as reference.
Extra virgin olive oil (EVOO) is defined as a functional food as it contains numerous phenolic components with well-recognized health-beneficial properties, such as high antioxidant and anti-inflammatory capacity. These characteristics depend on their structural/conformational behavior, which is largely determined by intra- and intermolecular H-bond interactions. While the vibrational dynamics of isolated compounds have been studied in a number of recent investigations, their signal in a real-life sample of EVOO is overwhelmed by the major constituent acids. Here, we provide a full characterization of the vibrational spectroscopic signal from commercially available EVOO samples using Inelastic Neutron Scattering (INS) and Raman spectroscopies. The spectra are dominated by CH2 vibrations, especially at about 750 cm(-1) and 1300 cm(-1). By comparison with the spectra from hydroxytyrosol and other minor phenolic compounds, we show that the best regions in which to look for the structure-activity information related to the minor polar compounds is at 675 and 1200 cm(-1) for hydroxytyrosol, and around 450 cm(-1) for all minor polar compounds used as reference, especially if a selectively deuterated sample is available. The regional origin of the EVOO samples investigated appears to be related to the different amount of phenolic esters versus acids as reflected by the relative intensities of the peaks at 1655 and 1747 cm(-1).

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