DOES ANTIAROMATICITY IMPLY NET DESTABILIZATION Academic Article uri icon

abstract

  • An analysis is presented of the results of earlier ab initio computational studies of cyclobutadiene, cyclooctatetraene, and 1,4dihydropyrazine. The first and third of these are normally categorized as antiaromatic. All three molecules are polyenes, even when the last two are forced into planar conformations. There is no driving force for extensive delocalization, even when it would appear to have been facilitated. Calculated isodesmic energies show a net destabilization only in the case of cyclobutadiene, which we attribute to strain and repulsion between the electrons of the CC double bonds. The other two molecules have negative isodesmic energies, indicative of net stabilizing effects. We conclude that the concept of antiaromaticity is useful for identifying molecules that resist the apparent opportunity for extensive delocalization, but that it does not intrinsically imply net destabilization. 1994 John Wiley & Sons, Inc. Copyright 1994 John Wiley & Sons, Inc.

published proceedings

  • INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY

author list (cited authors)

  • MURRAY, J. S., SEMINARIO, J. M., & POLITZER, P.

citation count

  • 30

complete list of authors

  • MURRAY, JS||SEMINARIO, JM||POLITZER, P

publication date

  • February 1994

publisher