Skip to main navigation Skip to search Skip to main content

Benzoquionones and related compounds. Part 2.1 Preferred conformations of some acyl-1,4-benzoquinones in solution

  • J. Malcolm Bruce
  • , Frank Heatley
  • , Roderick G. Ryles
  • , James Scrivens

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Studies based on polarographic reduction potentials, electronic absorption spectra, and 1H and 13C nuclear magnetic relaxation data show that in solution the preferred conformation of formyl-1,4-benzoquinone is that with the formyl and quinonoid groups coplanar, and the formyl carbonyl group anti to the 1-carbonyl, whereas that of acetyl- and pivaloyl-1,4-benzoquinone has the acyl groups approximately perpendicular to the quinonoid ring.

    Original languageEnglish
    Pages (from-to)860-866
    Number of pages7
    JournalJournal of the Chemical Society, Perkin Transactions 2
    Issue number6
    DOIs
    Publication statusPublished - 1 Jan 1980

    Fingerprint

    Dive into the research topics of 'Benzoquionones and related compounds. Part 2.1 Preferred conformations of some acyl-1,4-benzoquinones in solution'. Together they form a unique fingerprint.

    Cite this