Polyacetylenes mixed, conjugation

Similarly, cubic effects such as four-wave mixing, phase conjugation, and optical bistability form the basis of optical functions of strategic importance. In this case, materials such as polyacetylene could, in principle, compete effectively with inorganic solids such as gallium arsenide. 

Polyacetylene reacts with chlorine rapidly to give a white polymer that is equivalent to poly(l,2-dichloroethylene) and no stereospecificity has been reported on the chlorinated polymer. The addition of halogens is an important general reaction of carbon-carbon double bonds in a stereospecific and regiospecific sense. For instance, the electrophilic additions of chlorine to ethylene, buta-1,3-diene and hexa-l,3,5-triene have been shown to proceed by 1,2-trans (anti), 1,4-cis (syn) and 1,6-trans (anti) attack, respectively. This stereospecificity has been rationalized with a mixing rule of a-n orbital interaction. The reaction of a long conjugated polyene like polyacetylene with chlorine may produce an atactic chlorinated polyene, because random l,2n additions occur to result in a random addition product. ... 

Polypyrrole, polythiophene, polyaniline, polyfuran, polyacetylene, and poly-methylthiophene may exhibit a mixed electronic and ionic conductivity, similar to inorganic intercalation, or insertion compounds [43]. In the conductive form these polymers are partly oxidized and these positive charges are equilibrated by inorganic anions, which can diffuse through the polymer net. Alternatively, the conductive polymers can be partly reduced, with cations as counter ions. The eleetronic conductivity originates Irom partial oxidation of conjugated jt-bonds. The positive charge... 

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