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Jul 26, 2017 at 4:40 history edited j.c. CC BY-SA 3.0
fix broken images
Feb 14, 2012 at 0:24 history edited Joseph O'Rourke CC BY-SA 3.0
Fixed broken image link.
Nov 12, 2010 at 23:23 comment added J. M. isn't a mathematician Yes, there is a fair bit of, to use chemical terminology, steric and torsional strain in these. When Hückel aromaticity is good enough for Nature's purposes, there's really no need for Möbius.
Nov 12, 2010 at 20:15 history made wiki Post Made Community Wiki by S. Carnahan
Nov 12, 2010 at 20:01 comment added j.c. @Mariano: In naturally occuring reactions, (due to random collisions and the like) the products with lower energy will generically be preferred. The strain energy in these Möbius rings is high (due to the twisting; the $p_z$ orbitals prefer to be parallel (as that's what the lower energy π-bonding eigenfunctions look like)) compared to nontwisted rings.
Nov 12, 2010 at 16:25 history edited Joseph O'Rourke CC BY-SA 2.5
Added universal recycling sign for grins.
Nov 12, 2010 at 16:24 comment added Mariano Suárez-Álvarez Why don't they occur in nature?
Nov 12, 2010 at 16:16 comment added Joseph O'Rourke @J.M.: Thanks for the expert clarification!
Nov 12, 2010 at 16:07 comment added J. M. isn't a mathematician Möbius-aromatic compounds don't really occur in nature, though there is this Nature article on a compound with this property: dx.doi.org/10.1038/nature02224 . It is interesting that the concept was proposed in 1964, and only practically realized with the synthesis of a compound with this property nearly forty years later. (Yes, I'm a chemist. :) )
Nov 12, 2010 at 15:24 history answered Joseph O'Rourke CC BY-SA 2.5