An additivity scheme for conformational energies in substituted ethanes

Leo Radom*, Peter J. Stiles

*Corresponding author for this work

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Ab initio molecular orbital theory is used to demonstrate that conformational energies of polysubstituted ethanes may be well represented as linear combinations of conformational energies for ethane and appropriate mono- and 1,2-di-substituted derivatives.

Original languageEnglish
Pages (from-to)190-192
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number5
DOIs
Publication statusPublished - 1974
Externally publishedYes

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