Planar, methylene-bridged quinque- and septiphenyl oligomers were synt
hesized as soluble, hitherto unknown compounds. The series of homologo
us and planar ladder-type oligophenyls (ter-, quinque-, septiphenyl) w
as characterized especially with respect to their optical properties (
absorption and emission) as function of increasing chain length, and c
ompared to the corresponding ladder-type polyphenylene. An effective c
onjugation length of about 12 benzene rings was determined within this
series of planar oligo- and polyphenylenes.