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- W1972373023 abstract "Dihydroheptazethrene (V) and 1:14,11:12-dibenzo-5,7-dihydro-pentacene (VI) were synthesized. The former gave heptazethrene (VII) on dehydrogenation, whilst the latter polymerized immediately. This difference is explained by the fact that heptazethrene (VII) can be formulated with a Kekulé structure and the dehydrogenation product of VI cannot. Heptazethrene is a basis hydrocarbon and is closely related to dibenzoheptazethrene (VIII). Heptazethrenequinone (II) is a true quinone giving a blue vat, whilst the isomer (IV) is a diketone and does not give a vat." @default.
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- W1972373023 date "1962-01-01" @default.
- W1972373023 modified "2023-09-27" @default.
- W1972373023 title "The significance of Kekulé structures for the stability of aromatic systems—II" @default.
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- W1972373023 doi "https://doi.org/10.1016/s0040-4020(01)99296-8" @default.
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