The buckybowl trichalcogenasumanenes show cleavage of flanking benzene ring upon oxidation, which leads their dissection by fusing various amidine moieties onto peripheral region. By gradually increasing the ring size of amidine from five-to six-and seven-membered, the molecule engineering results in the [7-5-6]-, [7-6-6]-, and [7-7-6]fused polycycles. Three systems are distinct in the molecular geometries, packing motifs, and optoelectronic properties. The [7-5-6]-fused case adopts the flat backbone, displays strong emission with the fluorescence quantum yield up to 52.3 %, and undergoes a two-photon absorption process. The [7-6-6]-fused one is of a curvature with molecular geometry inversion, forms a tight stack of curved p-system, shows broad absorption extended to 700 nm, and exhibits the p-type semiconducting behavior with hole mobility of 4.4 x 10(-3) cm(2)V(-1) s(-1). The [7-7-6]-fused one possesses the highly twisted skeleton to show stable chirality, and exhibits red emission in both solution and solid state. The surgery on tri-chalcogenasumanene is a promising approach to create polycycles with diverse functionalities.
