Infrared spectra of all isomers of polymethyl-substituted benzoic acids were recorded in the carbonyl and hydroxyl regions in tetrachloromethane at various concentrations and interpreted in terms of conformation. According to a plot of #(C=O) of the monomeric form vs Hammett substituent constants ',
Far-infrared spectra of benzoic acid
β Scribed by H.R. Zelsmann; Z. Mielke
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 592 KB
- Volume
- 186
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Crystalline benzoic acid has been studied by far-infrared spectroscopy in the spectral region of 20-230 cm-' with a view to a determination and an assignment of the pure lattice and the intermonomer vibrations. An anomalous behaviour, similar to the one found earlier in the mid-IR, is observed for the asymmetric O-H...0 stretching band with regard to the numberofcomponents of the band and its changes as a function of temperature and deuteration. The experiments were carried out for single crystals of fully hydrogenated benzoic acid (-he) with polarization analysis, and for powder samples of h6, d,, d5 and d, benzoic acid at temperatures between 6 and 295 K. An explanation of these anomalies is proposed.
π SIMILAR VOLUMES
Far-infrared spectra in the region from 700 to 200 cm-l were measured for the copolymers of calanine and glycine, those of calanine and L-valine, those of calanine and L-leucine, and those of L-alanine and cphenylalanine. The observed spectra were interpreted on the basis of the analysis of the far-
Drboraroke de R&onance ~~f~gn&&e. D&arremenr de RedrercJxe Fondamenru!e. Cent-e d %rudes n'ickire~ de Grenoble-85X. F38ojl Grenoble Cede-q Fr~re Keceised 17 Ma)' 19S4; in final form 6 JuIy I984 The spectm of imidatok monocrysrals hxing their c nis (the average direction of H-lmndst in the obsmarion