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Copolymere aus Vinylchlorid und Kohlenmonoxid oder Sauerstoff wurden als Folien unter der Einwirkung von Wärme und Licht abgebaut. Mit zunehmendem Carbonylgehalt steigt die Instabilität der Polymeren. Der thermische Abbau wird durch Luftsauerstoff beschleunigt, der photolytische dagegen verzögert. Durch die Lichteinwirkung entstehen an der Folienoberfläche Polyensequenzen; tiefere Polymerschichten werden dadurch nicht geschädigt.

The electrooptical properties of side-chain liquid crystalline polymers were investigated for the case that the mesogenic units were attached laterally rather than longitudinally to a flexible chain backbone via flexible spacer units. The experimental finding is that these polymers display unusual electrooptical properties within the isotropic phase in the neighborhood of the transition into the nematic phase.The polymers are characterized by the occurrence of a fast and a slow electrooptical response both of which show a critical divergence of the Kerr constant and the Kerr relaxation time. In addition, they show dmiations between the rise and the decay values of the Kerr constants and in certain cases also of the Kerr relaxation times. Finally an overshoot of the induced birefringence following a sudden s t v i s e increase of the applied electric field has been found for one of these polymers. All these features can be accounted for on fhe basis of a newly developed theoretical approach that considers the particular dipolar and optical polarization configurations of these polymers. 1042-7147/90/01W93-09$05.~

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