## Abstract Average bond distances and bond angles in carboxylic esters with different substitution patterns have been derived by analyzing data from many crystal structures retrieved from the __Cambridge Structural Database__ (CSD). Conformationβal preferences in the attachment of substituents are
Structural Characteristics of the Carboxylic Amide Group
β Scribed by Pinakpani Chakrabarti; Jack D. Dunitz
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- German
- Weight
- 277 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
Average bond distances and bond angles as well as conformational preferences in the Ο and Ο torsion angles of carboxylic amides with different substitution patterns have been derived by analyzing data from many crystal structures retrieved from the Cambridge Structural Database (CSD).
π SIMILAR VOLUMES
The molecular organization of purely aromatic, polyphenyl carboxylic acids, as Langmuir monolayers at the air/water interface, has been investigated by means of surface pressure and electric surface potential measurements upon film compression. The monolayer characteristics of the basic compound, a