Author(s):
Fausto, R. 
; Martins, A. Gabriela ; Teixeira-Dias, J. J. C. ; Tonge, P. J. ; Carey, P. R.
Date: 1994
Persistent ID: http://hdl.handle.net/10316/18094
Origin: Estudo Geral - Universidade de Coimbra
Document details
Rotational Isomerism in CH3CH2-C(=S)SR (R = CH3, CH2CH3): A Combined Vibrational
Description
The vibrational and conformational properties exhibited by CHsCH2C(=S)SCHs and CH~CH~C(=S)SCHZCH3 were studied by Raman and infrared spectroscopies for the liquid and solid phases, and by ab initio calculations for the isolated molecule. It is shown that these molecules tend to adopt nonsymmetricconformations near the C(=S)S group, in contrast to their oxygen analogues whose most stable conformers correspond to structures having a planar skeleton. For the conformers differing by internal rotation about the C,-C bond, the most stable conformer-the skew form having the CC-C=S dihedral angle equal to flOOO-is more stable than the symmetric syn conformer (CC-C=S equal to Oo) by ca. 1.0 kJ mol-'. In the annealed solid, CH3CH*-C(=S)SCH3 exists in the skew conformation, which is also the most stable form in the liquid and isolated molecule. As the liquid is rapid-froze, a glassy state where both conformers exist is obtained, which enables a spectroscopic characterization of the less stable syn form, taking advantage of the usual solid-state band-narrowing effect. The conformational dependence of some relevant structural parameters was used to characterize the most important intramolecular interactions present in the various conformers. In addition, the ab initio vibrational spectra were calculated and used for the assignment of the experimentally observed bands. In particular, the Raman and IR spectra of the molecules in the liquid and solid phases were assigned and the results were used to explain details of the resonance Raman spectra of methyl dithiopropionate [Ozaki, Yo;St orer, A. C.; Carey, P. R. Can J. Chem. 1982, 60, 1901
The vibrational and conformational properties exhibited by CHsCH2C(=S)SCHs and CH~CH~C(=S)SCHZCH3 were studied by Raman and infrared spectroscopies for the liquid and solid phases, and by ab initio calculations for the isolated molecule. It is shown that these molecules tend to adopt nonsymmetricconformations near the C(=S)S group, in contrast to their oxygen analogues whose most stable conformers correspond to structures having a planar skeleton. For the conformers differing by internal rotation about the C,-C bond, the most stable conformer-the skew form having the CC-C=S dihedral angle equal to flOOO-is more stable than the symmetric syn conformer (CC-C=S equal to Oo) by ca. 1.0 kJ mol-'. In the annealed solid, CH3CH*-C(=S)SCH3 exists in the skew conformation, which is also the most stable form in the liquid and isolated molecule. As the liquid is rapid-froze, a glassy state where both conformers exist is obtained, which enables a spectroscopic characterization of the less stable syn form, taking advantage of the usual solid-state band-narrowing effect. The conformational dependence of some relevant structural parameters was used to characterize the most important intramolecular interactions present in the various conformers. In addition, the ab initio vibrational spectra were calculated and used for the assignment of the experimentally observed bands. In particular, the Raman and IR spectra of the molecules in the liquid and solid phases were assigned and the results were used to explain details of the resonance Raman spectra of methyl dithiopropionate [Ozaki, Yo;St orer, A. C.; Carey, P. R. Can J. Chem. 1982, 60, 1901
Document Type
Article
Language English
Language English
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