The new parent hydrocarbon 1 is the second cycloarene (after kekulene) that consists of twelve symmetrically arranged benzene rings. 1 forms yellow crystals and was prepared by photocyclization of a partially hydrogenated benzophenanthrenophanediene. Compound 1 contains 40 π electrons, but can be formulated with an inner and an outer [4n + 2] π-electron perimeter.
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Funhoff et al. (1986) studied this question.
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