Since the concept of aromaticity has been proposed to be generalizable to acetylenic rods ('linear ring' of [2]annulene), p-diisopropyl- tetraphenyl-carbo-benzene (C48H34) and an indenone-fused isopropyl- triphenyloctadehydro[14]annulene (C42H26O) can be regarded as based on heptacyclic aromatic cores. The formation and X-ray crystal structures of both products are described. The latter has been obtained as a reductive rearrangement product of a transient isopropyl-pentaoxy[ 5]pericyclyne devised as a putative precursor of a carbo-fulvene target. A mechanism accounting for this peculiar transformation is proposed. Deviation from global planarity is measured by a 6° angle between the mean plane of the indenone bicycle and that of 13 atoms of the [14]annulenic macrocycle, forming dihedral angles with the local plane of the isopropyl-substituted sp2 vertex of 16° and 15°, respectively. The magnetic aromaticity of the carbo-benzene and indeno-octadehydro[ 14]annulene products is evaluated by NICS calculations. [ABSTRACT FROM AUTHOR]