| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5374733 | Chemical Physics | 2011 | 7 Pages |
Abstract
⺠Glycine conformational preferences in the isolated state were fully investigated. ⺠The lowest energy conformation is not stabilized by hydrogen bonding. ⺠Steric and hyperconjugative effects were analyzed for all conformers. ⺠Several theoretical methods were used to explain the conformational preferences.
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Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Rodrigo A. Cormanich, Lucas C. Ducati, Roberto Rittner,