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• W2037344037 endingPage "293" @default.
• W2037344037 startingPage "282" @default.
• W2037344037 abstract "The molecular characteristics of two naturally occurring flavonoid compounds mearnsetin and myricetin have been computed using density functional theory (DFT) approach with B3LYP/6-311G(d,p) level of theory. The computation and analysis of bond dissociation enthalpy magnitudes for all the OH sites for both the compounds clearly denotes the contribution of the B-ring for the antioxidant activity. The analysis has also indicated the higher values of BDE on the C5-OH radical species in both the compounds. The computed vibrational frequency analysis indicates the absence of imaginary frequency in the neutral as well as radical species of both the flavonoid compounds. The ionisation potential (IP) analysis was found to be within the range of the IP of synthetic food additives. In addition, various molecular descriptors such as electron affinity, hardness, softness, electronegativity, electrophilic index have also been calculated and the validity of Koopman's theorem is verified. The plot of frontier molecular orbital and spin density distribution analysis for neutral and the corresponding radical species for both the compounds have been computed and interpreted. The polar nature and their polarizing capacity are well established through the analysis of dipole moment and polarisability magnitudes." @default.
• W2037344037 created "2016-06-24" @default.
• W2037344037 creator A5056983586 @default.
• W2037344037 creator A5069975547 @default.
• W2037344037 date "2011-06-01" @default.
• W2037344037 modified "2023-10-06" @default.
• W2037344037 title "Antioxidant behavior of mearnsetin and myricetin flavonoid compounds — A DFT study" @default.
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• W2037344037 doi "https://doi.org/10.1016/j.saa.2011.02.042" @default.
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• W2037344037 hasPublicationYear "2011" @default.
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