Vibrational circular dichroism of gramicidin D in organic solvents
β Scribed by Chunxia Zhao; Prasad L. Polavarapu
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 161 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1075-4261
No coin nor oath required. For personal study only.
β¦ Synopsis
The vibrational circular dichroism (VCD) and absorption spectra of gramicidin D in different organic solvents are presented in the amide I and II regions. The absorption and VCD spectra suggest that gramicidin structures are similar in dioxane and chloroform. However, the structures adopted by gramicidin in chloroform are due to the trace amount of protective ethanol present in chloroform solvent. In the absence of this protective ethanol, gramicidin appears to aggregate in chloroform. The gramicidin structures appear to be similar in propanol and ethanol, but the composition of these structures appear to be different from those in dioxane and chloroform. In methanol-d 4 , a different composition of structures, including monomers, appears to be present. The structures in dimethyl-d 6 -sulfoxide and 2,2,2-trifluoroethanol are entirely different from those in all other solvents.
π SIMILAR VOLUMES
Vibrational circular dichroism (VCD), the differential absorption of circularly polarized light by vibrational transitions, is a new technique of potential use for stereochemical analysis.13 Recent instrumental developments have allowed extension of the VCD technique down to 1250 cm-l, thereby encom
The Raman and absorption spectra of tetraphenylporphyrin (TPP) were calculated and compared to experiment. The computation was based on the harmonic molecular force field and electric tensors obtained ab initio at the BPW91/6-31G\* level. Good agreement was found between experimental and calculated
## Abstract The vibrational absorption and vibrational circular dichroism (VCD) spectra of melittin in D~2~O solutions at different pH values, different salt concentrations, or different 2,2,2βtrifluoroethanol (TFE) concentrations are recorded in the amide Iβ² (1850β1600 cm^β1^) region. Two models a
## Abstract The vibrational circular dichroism (VCD) and IR absorption spectra of a dodecamer d(CCTCTGGTCTCC)Β·d(GGAGACCAGAGG) coordinated with cisplatin are distinct compared to those of the dodecamer without cisplatin. Although the intensity of PO~2~/deoxyribose absorptions (1150β850 cm^β1^) incre