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- W4289929682 abstract "Dispersion correction in theoretical determination of cyclopeptide conformations is emphasized. Whether in gas approximation or in solvation simulation, the density functional theory with London dispersion correction (DFT-D3) demonstrates that only 2-3 conformers can stably coexist for cycloaspeptides (A, D, G) at B3LYP-D3 and CAM-B3LYP-D3. Conformational rationality is confirmed by electronic circular dichroism (ECD). Whether for Cotton effect or for excitation energy, TD-B3LYP-D3 has better performances than TD-CAM-B3LYP-D3 because the former can better reproduce the experiment. A molecular orbital analysis is used to interpret ECD, where two energy bands observed in experiment originates from the ππ* transitions other than the σπ* transitions. Long-range correction and solvent effect make H-bonds shorten, and dispersion correction makes them further shorten." @default.
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- W4289929682 date "2022-12-01" @default.
- W4289929682 modified "2023-10-10" @default.
- W4289929682 title "Upon DFT-D3 dispersion correction and ECD spectral confirmation, only several conformers can stably coexist for three fungal cycloaspeptides (A, D, G)" @default.
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- W4289929682 doi "https://doi.org/10.1016/j.saa.2022.121710" @default.
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