Radiolytic preparation, chromatographic resolution and absorption spectra of cis- and trans-1-iodopropene

R. H. Schuler, L. Wojnárovits

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

1-Iodopropene has been prepared in its cis and trans configurations by scavenging the 1-propenyl radical produced in the dissociative attachment of electrons to cis- and trans-1-bromopropene with iodine. Gel permeation methods have been used to separate these two isomers. The chromatographic data show that identical ratios of these isomers are produced from each of the 1-bromopropene isomers as the result of interchange of the cis and trans configurations of the vinyl like 1-propenyl radical on a time scale shorter than that for the scavenging process, i.e.,

Original languageEnglish
Pages (from-to)219-224
Number of pages6
JournalRadiation Physics and Chemistry
Volume67
Issue number3-4
DOIs
Publication statusPublished - Jun 1 2003

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isomers
scavenging
absorption spectra
preparation
configurations
iodine
attachment
gels
electrons

Keywords

  • 1-Propenyl radical
  • cis/trans-1-Iodopropene
  • Gel permeation chromatographic analysis
  • Hydrocarbon radiolysis
  • Radical scavenging

ASJC Scopus subject areas

  • Radiation

Cite this

Radiolytic preparation, chromatographic resolution and absorption spectra of cis- and trans-1-iodopropene. / Schuler, R. H.; Wojnárovits, L.

In: Radiation Physics and Chemistry, Vol. 67, No. 3-4, 01.06.2003, p. 219-224.

Research output: Contribution to journalArticle

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