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Absorbance shift, conducting polymer

The carbazole group absorbs light in the UV range. Therefore, polymers of this type can become photo-conductive as such only in the UV range. However, colored sensihzers can be added to shift the photoconduchvity into the visible region. [Pg.13]

Analogous to PTs, pyrrole polymers have been polymerized from the dimer with similar results. For example, poly(JV,JV -dimethyl-2,2 -bipyrrole), poly(NNDMBP) (24) exhibits a blue-shifted onset of absorbance of the neutral polymers [94-96]. This results in an increased visible region transparency of the film in the neutral state. The polymer is pale, transmissive yellow in the neutral state and switches to gray-blue when oxidized. In addition, the dimer oxidizes at a lower oxidation potential and the resulting polymer film has an increased conductivity over that produced from the monomer. [Pg.857]

Electrosynthesized polymers of TV-methylpyrrole (NMPy) and A -methylpyrrole-2,6-dimethyl-P-cyclodextrin (NMPy P-DMCD) were characterized with cyclic voltammetry and in situ conductivity measurements in aqueous and nonaqueous solutions [23]. In situ UV-vis-spectra of PNMPy and poly(NMPy-P-DMCD) films show differences both in band absorbances and in energies of polaronic transitions. SUght positive potential shifts are observed for poly(NMPy-P-DMCD) in aqueous and nonaqueous solutions compared to PNMPy films. This observation may be a result of the hydrophobic monomer NMPy, partly or entirely included in the CD s hydrophobic cavity. The results of in situ conductivity measurement for films in this investigation indicate that the resistivity of films that prepared in nonaqueous solution in acetonitrile + LiC104 are lower than resistivity of films prepared in LiC104 aqueous solution by approximately an order of magnitude. [Pg.1510]


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