Conformational studies of poly(N-methyl-l-alanine) by n.m.r. spectroscopy
β Scribed by Yukio Imanishi; Kazuya Kugimiya; Toshinobu Higashimura
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 416 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0032-3861
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π SIMILAR VOLUMES
Sterically allowed forms of the poly-N-methyl-calanine chain were found by calculation of conformational energies as a function of the rotation angles of its chain bonds. The lowest energy form seems to be a right-handed, approximately threefold helix.
Conformational energies of the poly-N-methyl-halanine chain have been calculated as a function of the rotational angles of its skeletal bonds, taking into account torsional potentials, van der Waals repulsions, and London attractions. Four pronounced minima in the energy were found; the relative mag
High-resolution nuclear magnetic resonance spectra at 100 MHz have been obtained on poly-iV-methyl-L-alanine in the chloroform-trifluoroacetic acid system under various conditions of solvent composition. Different spectra are observed for the CH,-C,, C,-H, and N-CHI protons. On the basis of conforma
## Abstract Polymerizations of Lβ and DLβphenylalanine __N__βcarboxyanhydride in nitrobenzene by poly (__N__βmethylβLβalanine) of varying degrees of polymerization (__n__ = 1β30) were investigated. Poly(__N__βmethylβLβalanine) was prepared by the polymerization of __N__βmethylβLβalanine NCA with __