We have investigated the properties of thin films of a substituted polypyrrole synthesized via the chemical
oxidation of a chloroform solution of 5-acetamido-4,5,6,7-tetrahydro-2H-benzo[c]pyrrole. Repeated compressions of Langmuir films prepared by spreading a dilute chloroform/dimethyl sulfoxide solution of the
polymer at an air−water interface have established their long-term stability as floating monolayers.
Hysteresis experiments and surface potential measurements have indicated that while the stiff condensed
layer changes its structure upon the first compression, the size and distribution of floating domains remain
invariant under subsequent cycles of compression and decompression. An infrared spectroscopic investigation
was carried out for KBr mixed pellets of the material and for Langmuir−Blodgett (LB) films obtained by
depositing six monolayers of the polymer on ZnSe crystals. The presence of a broad bipolaron band both
in the transmission and in the attenuated total reflection (ATR) spectra indicates that in its pristine form
the polymer was already slightly doped, a hypothesis confirmed by preliminary two-probe measurements.
To better understand the nature of the organization of the deposited films we performed a linear dichroism
analysis of the polarized ATR spectra and found evidence that the polymeric chains are transferred in a
helical manner along the surface of the substrate.