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Tabrizi, M.Z. et al.

Fourier transform infrared and Raman spectra, vibrational assignment and density functional theory calculations of naphthazarin.

FT Raman and FTIR spectra of Naphthazarin (5,8-dihydroxy-1,4-naphthoquinone) and its deuterated analogue are recorded. Comparison between the spectra obtained by two techniques, a series of density functional theory (DFT) calculations and the spectral behavior upon deuteration were used for the assignment of the vibrational spectra of this compound. The calculated vibrational frequencies by the B3LYP, B3PW91, G96LYP, G96P86, and MPWLYP density functionals are generally consistent with the observed spectra. Infrared and Raman vibrational transitions predicted by B3LYP/6-311++G** are reported for the titled compound and its deuterated analogous and the assignments are discussed. All experimental and theoretical results support a relatively weak hydrogen bond in naphthazarin (NZ), compared with that in the enol form of normal beta-diketones. The observed nuOH/nuOD and gammaOH/gammaOD appear at about 3060/2220 and 790/560 cm(-1), respectively, which are consistent with the calculated hydrogen bond geometry and proton chemical shift results. Two bands at about 350 and 290 cm(-1) are assigned to the O...O stretching modes belong to A1 and B2 species, respectively.[1]

References

Fourier transform infrared and Raman spectra, vibrational assignment and density functional theory calculations of naphthazarin. Tabrizi, M.Z., Tayyari, S.F., Tayyari, F., Behforouz, M. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. (2004) [Pubmed]

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