Materials with a ribbon- or ladder-type framework possess a two-dimensional
geometry and are thus intermediate between linear and three-dimensional sy
stems. The limited conformational freedom of ladder polymers is particularl
y relevant in the case of conjugated ladder-type materials since the steric
inhibition of electron delocalization is drastically reduced.
Up until today two general routes have been used to prepare ladder-type mat
erials: (1) the polymerisation of multifunctional monomers, in which both s
trands of the ladder structure are generated in a single reaction; and (2)
the cyclisation of suitably functionalized open-chain (single-stranded) pre
cursor polymers in a polymer-analogous process. Both strategies pre-suppose
certain essentials to arrive at structurally defined ladder polymers, espe
cially the exclusion of side-reactions and an almost quantitative conversio
n of the starting materials.
The main attention of this article is focused on an active physical functio
n of ladder-type materials. Among others, ladder-type poly(p-phenylene)s (L
PPPs) represent an outstanding class of ladder-type materials. They are cha
racterized by an extraordinarily low concentration of active traps (topolog
ical defects, impurities) and display a set of attractive electronic proper
ties (very intensive photo- and electroluminescence, high charge carrier mo
bilities). This unique performance has established the solution processable
LPPPs as standard materials for organic polymer based light emitting diode
s (LEDs) and optically pumped solid state lasers.