Does Antiaromaticity Imply Destabilization

Abstract

An analysis is presented of the results of earlier ab initio computational studies of cyclobutadiene, cyclooctatetraene and 1,4- dihydropyrazine. 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 pi 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 pi electrons. of the C=C 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 resis the apparent opportunity for extensive pi delocalization, but that it does not intrinsically imply net destabilization.

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Document Details

Document Type
Technical Report
Publication Date
Dec 27, 1993
Accession Number
ADA274622

Entities

People

  • Jane S. Murray
  • Jorge M. Seminario
  • Peter Politzer

Organizations

  • University of New Orleans

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Abstracts
  • Alkenes
  • Chemical Compounds
  • Chemistry
  • Classification
  • Cyclooctatetraene
  • Electrons
  • Governments
  • Ground State
  • Military Research
  • Molecules
  • Physical Properties
  • Quantum Chemistry
  • United States
  • United States Government
  • Wave Functions

Readers

  • Quantum Chemistry
  • Strategic Security Studies

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene