The synthetic polymer poly-L-proline exists in two conformational forms, I and 11, the structures of which have been elucidated by x-ray crystallography.'-3 Form I is a right-handed helix with all peptide bonds in the cis configuration, and is stable in pyridine and aliphatic alcohols. Form I1 is a
A vibrational study of poly (L-proline) I and II in the far infrared
β Scribed by John F. Rabolt; William Wedding; Kenneth W. Johnson
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1975
- Tongue
- English
- Weight
- 421 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Abstract
The far infrared spectra of poly(Lβproline) I (190β35 cm^β1^) and II (400β35 cm^β1^) were obtained in the solid state at both 300Β° and 110Β°K. A significant difference in the region below 100 cm^β1^ was observed. A very intense band located at 60 cm^β1^ in the infrared spectrum of form II has no counterpart in form I. This indicates the sensitivity of lowβfrequency vibrations to the difference in conformation assumed by both forms in the solid state.
Additional bands observed in this study are correlated with ir and Raman data previously reported and tentative assignments are made using the results of normal mode calculations (in the singleβchain approximation) which have been reported.
π SIMILAR VOLUMES
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The infrared absorption of poly-L-proline in concentrated aqueous salt solutions was measured in the fundanierital region. Of primary interest were the carbonyl absorption of the peptide linkage and the methylene C-H bending absorption of the pyrrolidine ring. These spectral regions each show an add
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