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, th
Infrared and Raman spectra of L-valine nitrate and L-leucine nitrate
β Scribed by Beulah J. M. Rajkumar; V. Ramakrishnan
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 95 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0377-0486
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β¦ Synopsis
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 several modes of vibrations were shifted from the expected values in both crystals. The removal of degeneracy of certain modes of vibration of the methyl group suggests that the two methyl groups attached to the same carbon atom are not identical and the symmetry of both of these groups was affected in their respective environments.
π SIMILAR VOLUMES
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
## Abstract __Cyclo__(DβLeuβLβLeu) and __cyclo__(LβLeuβLβLeu) were synthesized, and their carbonβ13 nmr spectra at 65 MHz were examined in dimethylsulfoxide and trifluoroacetic acid solutions. The chemical shift data are consistent with a boat or βtwistedβ boat conformation of the diketopiperazine