Dithieno[3,4-b:3',4'-d]thiophene-annelated antiaromatic planar cyclooctatetraene with olefinic protons

Org Lett. 2013 Jul 19;15(14):3522-5. doi: 10.1021/ol401125f. Epub 2013 Jul 9.

Abstract

The design and synthesis of a new planar cyclooctatetraene (COT) with protons directly connected to the COT ring was attained by monoannelation with dithieno[3,4-b:3',4'-d]thiophene. The planar structure of the COT core was unambiguously confirmed by X-ray crystallography. The magnetic antiaromaticity of the COT core was found to be higher than that of the previously synthesized planar COTs with olefinic protons, according to the results of (1)H NMR and absorption spectra as well as NICS calculations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Crystallography, X-Ray
  • Cyclooctanes / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Protons
  • Thiophenes / chemistry*

Substances

  • Alkenes
  • Cyclooctanes
  • Protons
  • Thiophenes
  • 1,3,5,7-cyclooctatetraene