Abstract
Unusually large lanthanide-induced shifts are observed for proton resonances of methoxy, ethoxy and dimethylamino substituents peri to carbonyl groups of anthraquinones and naphthoquinones. Such an arrangement allows the substrate to act as a bidentate ligand and is evidently the favoured site of coordination.
Original language | English |
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Pages (from-to) | 1255-1258 |
Number of pages | 4 |
Journal | Australian Journal of Chemistry |
Volume | 30 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Jan 1977 |
Externally published | Yes |