A molecular orbital study of the conformation of formycin
β Scribed by Daniel W. Miles; Douglas L. Miles; H. Eyring
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 416 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-5193
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
study of peroxyacetic acid has been performed using both STO-3G and PCLO moIecuk orbital r&hods. The tot&y planar, cis conformer is obtained by both methods and is consistent with X-ray, infrwed;and dipole moment results. : '.(.VOlu&. 32, number z
The conformational characteristics of allylamine were investigated by the ab initio STO-~G basis set. The results indicate that the molecule exists in a number of stable conformations through rotations about the CC-NH and CC-CN bonds. The TE ( &u~-CCNLP, LP representing lone-pair electrons, and ecli