Polycarbazole (PCz) was synthesized by chemical polymerization of carbazole in acetonitrile medium using ammonium persulfate as oxidant. The selection of solvent, concentration of the monomer, composition of the solvent, polymerization time, temperature, and pH were optimized to obtain better quality and yield of the polycarbazole. The synthesized polycarbazole was characterized by various techniques such as UV-Visible, FTIR, 1 H-NMR, 13 C-NMR, COSY, NOESY, and XRD spectroscopy. The solubility of the polycarbazole was tested in various solvents. The thermodynamic stability of the polycarbazole was examined by DSC and TGA-DTA analysis.

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Conducting copolymers of imidazole and carbazole were chemically synthesized in various molar ratios of the imidazole and carbazole by chemical oxidative polymerization in acetonitrile medium using ammonium persulphate as oxidant. The selection and composition of solvent, concentration of the monomer, polymerization time, and temperature were optimized to obtain better quality and yield of the copolymers. The synthesized conducting copolymers were characterized by various techniques such as UVvisible, Fourier transform infrared, 1 H-NMR, and X-ray diffraction spectroscopy. The solubility of the copolymers was tested in various solvents. Their conductivity was tested at various temperatures. The thermodynamic stability of the copolymers was examined by differential scanning colorimetric and thermogravimetric analysis. The copolymers show comparatively higher conductivity, better solubility, and higher thermal stability than the homopolymer poly(carbazole) and lower than that of poly(imidazole).

A series of conducting copolymers were synthesized by chemical oxidative polymerization of imidazole (Imi) and pyridine (Py) in acetonitrile medium at ambient temperature. The yield, solubility, and conductivity of the copolymers were measured by changing the Imi/Py molar ratio from 0/100 to 100/0. The as-prepared Imi/Py conducting copolymers were characterized by UVVisible, FTIR, 1 H-NMR, DSC, TGA, and XRD. The results suggest that the resulting copolymers were more easily soluble in most of the organic solvents than in polyimidazole. The polymer obtained is a real copolymer containing imidazole and pyridine units, but the Imi content calculated on the basis of the proton NMR spectra is lower than feed Imi content. The thermostability of the Imi/Py copolymer increases with increasing Imi unit content. The copolymers show comparatively higher conductivity and higher thermal stability than the homopolymer polypyridine and are lower than those of polyimidazole.

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