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Article Abstract
Structural, conformational, and spectroscopic investigations of methyl-eugenol were made theoretically at the IR, Raman, and UV-vis spectra were investigated and analyzed in light of the computed quantities. Conformational analysis was carried out with the help of total energy vs. dihedral angle curves for different tops, yielding 21 stable conformers, out of which only two have energies below the room temperature relative to the lowest energy conformer. The effect of the solvent on different molecular characteristics was investigated theoretically. MEP and HOMO-LUMO analysis were carried out and barrier heights and bioactivity scores were determined. The present investigation suggests that the molecule has three active sites with moderate bioactivity. The solvent-solute interaction is found to be dominant in the vicinity of the methoxy moieties.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386374 | PMC |
| http://dx.doi.org/10.3390/molecules28145409 | DOI Listing |
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