Antiaromaticity in Relation to 1,3,5,7-Cyclooctatetraene Structures

Abstract

An isodesmic energy analysis has been carried out at the MP2/6-31G*// HF/3-21G level for the non-planar ground state (1) of 1,3,5,7-cyclooctatetraene and for two planar forms, one having complete pi delocalization (2) and the other having alternating single and double bonds (3). 1 is found to have a considerable degree of stabilization, which is attributed to limited pi delocalization. The polyene 3 is the more stable of the two planar forms; it is a transition state in the inversion between two possible non-planar structures. 2 is found to be a triplet at the Hartree-Fock level, and is a critical point on an alternate pathway between the two possible arrangements of alternating single and double bonds in 3. Both 2 and 3 have negative isodesmic energies, indicating the presence of stabilizing factors.

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Document Details

Document Type
Technical Report
Publication Date
Dec 27, 1993
Accession Number
ADA274636

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
  • Acyclic Hydrocarbons
  • Alkenes
  • Chemical Compounds
  • Chemistry
  • Cycloalkenes
  • Cyclooctatetraene
  • Electrons
  • Ethylenes
  • Frequency
  • Hydrocarbons
  • Military Research
  • Molecules
  • Organic Compounds
  • United States
  • United States Government

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