Macrocyclic bis-dienes and diendienophile were prepared in Diels-Alder
reactions starting from the bis-dienophilic (hemiporphyrazinato)nicke
l complex 1. Compound 1 was reacted either with the tetraene 2 or with
tetraphenylcyclopentadienone (4). By combination of macrocyclic bis-d
ienes and bis-dienophiles, ladder-type oligomers (e.g. 9 or 10) were s
ynthesized. The described oligomers are precursors for the correspondi
ng conjugated oligomers, which are of interest as organic conductors.
The preparation of the corresponding phthalocyanine compounds e.g. 13-
16 and a method for obtaining the wanted ''D-2h'' phthalocyanine 19 wi
thout using tedious methods are reported.