Hyperconjugation not steric repulsion leads to the staggered structure of ethane

Vojislava Pophristic and Lionel Goodman ()
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Vojislava Pophristic: Wright and Rieman Chemistry Laboratories, Rutgers University
Lionel Goodman: Wright and Rieman Chemistry Laboratories, Rutgers University

Nature, 2001, vol. 411, issue 6837, 565-568

Abstract: Abstract Many molecules can rotate internally around one or more of their bonds so that during a full 360° rotation, they will change between unstable and relatively stable conformations. Ethane is the textbook example of a molecule exhibiting such behaviour: as one of its two methyl (CH3) groups rotates once around the central carbon–carbon bond, the molecule will alternate three times between an unstable eclipsed conformation and the preferred staggered conformation. This structural preference is usually attributed to steric effects1,2,3,4,5,6,7; that is, while ethane rotates towards an eclipsed structure, the electrons in C–H bonds on the different C atoms are drawing closer to each other and therefore experience increased repulsion, introducing a rotation barrier that destabilizes the eclipsed structure8,9. Stabilization of the staggered structure through rotation-induced weakening of the central C–C bond10 and hyperconjugation11,12 has been considered to be involved, but evaluation of the contributions of these effects to ethane's internal rotation barrier and conformational preference remains difficult13,14. Here we report a series of ethane structure optimizations, where successive removal of different interactions indicates that ethane's staggered conformation is the result of preferential stabilization through hyperconjugation. Removal of hyperconjugation interactions yields the eclipsed structure as the preferred conformation, whereas repulsive forces, either present or absent, have no influence on the preference for a staggered conformation.

Date: 2001
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DOI: 10.1038/35079036

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