Beta-Thioxoketones: Part 8. X-Ray Photoelectron Spectroscopic Study of the Enol-Enethiol Tautomerism of Thioacetylacetone and Related β-thioxoketones

F. S. Jørgensen, R. S. Brown, Lars Carlsen, F. Duus

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    X-ray photoelectron spectroscopy has been used to record the 01, and Szp ionization spectra of thioacetylacetone, 2-acetylcyclohexanethione,2 -thioacetylcyclohexanone,th e S-methyl derivative of thioacetylacetone, and propyl 3-mercaptocrotonate in the gas phase. It is shown that both the enol and the enethiol tautomers of the /3-thioxoketones can be detected, and the
    enol/enethiol ratios for thioacetylacetone, 2-acetylcyclohexanethione, and 2-thioacetylcyclohexanone were determined to be 61:39, 30:70, and 80:20, respectively, based on the intensities of the oxygen ionizations. The conclusions derived from the sulfur region support the above, although they are less clear due to sulfur spin-orbit splitting. The enol/enethiol ratios obtained in the gas phase by XPS are compared with data from other methods, showing good agreement between results obtained in the gas phase and in solution. The binding energy (BE) shifts of the O,, and Szp orbitals have been discussed and suggest that geometrical factors affect the strength of the intramolecular hydrogen bond.
    Original languageEnglish
    JournalJournal of the American Chemical Society
    Volume104
    Issue number22
    Pages (from-to)5922-5926
    ISSN0002-7863
    DOIs
    Publication statusPublished - 1982

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