Conformational preferences of Criegee intermediates: Isopropyl substituted carbonyl oxide

Carlos Cabezas, Jean-Claude Guillemin, Yasuki Endo*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Three conformers of the isopropyl-substituted Criegee intermediate, (CH3)(2) CHCHOO, have been observed by Fourier transform microwave spectroscopy. The transient species was produced using a pulsed electric discharge of a gas mixture of 1,1-diiodo-2-methylpropane/O-2 diluted in Ar or Ne. The use of different carrier gases in the supersonic expansion reveals the difference of the collisional relaxation process between anti-conformers. The conformational relaxation pathways have been investigated theoretically and are presented as well. In light of these results, the previous study on the ethyl-substituted Criegee intermediate, where the absence of one of the four possible conformers was associated with collisional relaxation processes, has been re-examined. Here we report the detection of a new conformer of the ethyl-substituted Criegee intermediate observed using Ne as the seeding gas. Published by AIP Publishing.

Original languageEnglish
Article number084309
Number of pages6
JournalJournal of Chemical Physics
Volume149
Issue number8
DOIs
StatePublished - 28 Aug 2018

Keywords

  • VOLATILE ORGANIC-COMPOUNDS
  • CONFORMER-DEPENDENT REACTIVITY
  • TROPOSPHERIC CHEMISTRY
  • KINETICS
  • SPECTROSCOPY
  • (CH3)(2)COO
  • DEGRADATION
  • CH3CHOO
  • CH2OO

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