A comparative study of the infrared and Raman spectra of L-valine nitrate and L-leucine nitrate helps in determining the role of hydrogen bonds in these crystals. Both compounds have carboxylic and protonated amino groups in the cation while the nitrate ion forms the anion. The wavenumbers of severa
Infrared and Raman spectra of DL-histidinium dinitrate and L-histidinium sulphamate
โ Scribed by Beulah J. M. Rajkumar; V. Ramakrishnan; S. Asath Bahadur
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 92 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0377-0486
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โฆ Synopsis
A comparative study of the infrared and Raman spectra of DL-histidinium dinitrate and L-histidinium sulphamate helps in determining the effect of hydrogen bonding in these crystals. The nitrate compound has a carboxylic group whereas the sulphamate compound has an ionized carboxyl group. However, the protonated imidazolium ring makes the histidine group in both cases ionic. Several group wavenumbers have been shifted in both molecules, indicating extensive hydrogen bonding. Some of the forbidden modes of the nitrate group have been observed. The removal of degeneracy of certain modes of both the nitrate and sulphamate anions suggests that the symmetry of both of these groups have been affected in their respective environments.
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The infrared and Raman spectra of polycrystalline were recorded at 77 and 10 K, respectively. (CH 3 ) 3 CCCH Crystal splittings were observed for some of the fundamentals and possible crystal structures are discussed. Anomalous band shifts between the liquid and solid state spectra were noted for bu
Polarized Raman spectra of the new weak ferroelectric crystal cyclohexane-1,1 -diacetic acid [C 6 H 10 (CH 2 COOH) 2 ] were studied in the temperature range 300-420 K and spectral range 10-3500 cm -1 . Wavenumbers of external modes were compared with the modes observed in far-infrared transmission s