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 language | English |
|---|---|
| Pages (from-to) | 860-866 |
| Number of pages | 7 |
| Journal | Journal of the Chemical Society, Perkin Transactions 2 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Jan 1980 |
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