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Chiroptical properties of unsaturated peptides

โœ Scribed by Osvaldo Pieroni; Adriano Fissi; Giorgio Montagnoli


Publisher
Wiley (John Wiley & Sons)
Year
1973
Tongue
English
Weight
165 KB
Volume
12
Category
Article
ISSN
0006-3525

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โœฆ Synopsis


It is known that rigid short range structures such as certain model amides' and diketopiperazinesz can produce ORD and CD spectra with Cotton effects somewhat similar to those displayed by stereo-ordered macromolecules. In this connection, unsaturated peptides,3 in which the rigidity of the chain is enhanced by the carbon-carbon double bond, can be of particular interest.

In the present preliminary communication some features are reported concerning absorption, ORD, and CD spectra in the near U.V. of six N-acylated unsaturated peptides containing one (I) or two (11) dehydrophenylalanyl residues and having respectively C-terminal Lalanine (A), bphenylalanine (Ph), and L-glutamic acid (G) residues.


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## Abstract The chiroptical properties of Sโ€proline conformational isomers are examined on a theoretical model in which electronic wave functions are obtained from semiempirical molecular orbital calculations. The CNDO/S molecular orbital model is used to perform SCFโ€MO calculations on ground state