FT‐Raman, FT‐IR spectra and DFT calculations on monomeric and dimeric structures of 5‐fluoro‐ and 5‐chloro‐salicylic acid

Journal of Raman Spectroscopy - Tập 41 Số 9 - Trang 1085-1097 - 2010
M. Karabacak1, Etem Kose1, Mustafa Kurt2
1Department of Physics, Afyon Kocatepe University, TR-03040 Afyonkarahisar, Turkey
2Department of Physics, Ahi Evran University, TR-40100 Kırşehir, Turkey

Tóm tắt

AbstractThe experimental and theoretical study on the structures and vibrations of 5‐fluoro‐salicylic acid and 5‐chloro‐salicylic acid (5‐FSA and 5‐ClSA, C7H5FO3 and C7H5ClO3) is presented. The Fourier transform infrared spectra (4000–400 cm−1) and the Fourier transform Raman spectra (4000–50 cm−1) of the title molecules in the solid phase were recorded. The molecular structures, vibrational wavenumbers, infrared intensities, Raman intensities and Raman scattering activities were calculated for a pair of molecules linked by the intermolecular OH···O hydrogen bond. The geometrical parameters and energies of 5‐FSA and 5ClSA were obtained for all eight conformers/isomers from density functional theory (DFT) (B3LYP) with 6‐311++G(d,p) basis set calculations. The computational results identified the most stable conformer of 5‐FSA and 5‐ClSA as the C1 form. The complete assignments were performed on the basis of the total energy distribution (TED) of the vibrational modes, calculated with scaled quantum mechanics (SQM) method. The spectroscopic and theoretical results were compared with the corresponding properties for 5‐FSA and 5‐ClSA monomers and dimer of C1 conformer. The optimized bond lengths, bond angles and calculated wavenumbers showed the best agreement with the experimental results. Copyright © 2010 John Wiley & Sons, Ltd.

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Journal of Raman Spectroscopy

Tập 41 Số 9

1085-1097

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