Indenone and cyclopentadienone energetics via mass spectrometry and computations: Are these species antiaromatic or "merely" nonaromatic?

Alireza Fattahi, Joel F. Liebman, Margarida S. Miranda, Victor M.F. Morais, M. Agostinha R. Matos, Lev Lis, Steven R. Kass

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The heat of hydrogenation of indenone was measured via two partially independent thermodynamic cycles by carrying out energetic measurements (i.e., electron affinities, proton affinities and ionization potentials) on both negative and positive ions (ΔH°H2 = 17.8 ± 5.5 and 17.5 ± 5.7 kcal mol-1, respectively). High level G3 computations were also carried out to provide the heats of formation of indenone (16.8 kcal mol-1) and cyclopentadienone (14.0 kcal mol -1). These 4n π electron systems are found to be nonaromatic in contrast to previous views. A recent report on cyclopropenyl anion (J. Org. Chem. 2013, 78, 7370-7372) indicates that this ion is also nonaromatic, and suggests that NMR ring currents and nucleus independent chemical shift (NICS) calculations do not correlate with the energetic criterion for antiaromatic compounds.

Original languageEnglish (US)
Pages (from-to)87-91
Number of pages5
JournalInternational Journal of Mass Spectrometry
Volume369
DOIs
StatePublished - Aug 15 2014

Bibliographical note

Funding Information:
Support from the National Science Foundation and the Minnesota Supercomputer Institute for Advanced Computational Research are gratefully acknowledged.

Keywords

  • Antiaromaticity
  • Cyclopentadienone
  • FTMS
  • Heat of hydrogenation
  • Indenone

Fingerprint

Dive into the research topics of 'Indenone and cyclopentadienone energetics via mass spectrometry and computations: Are these species antiaromatic or "merely" nonaromatic?'. Together they form a unique fingerprint.

Cite this