Among conducting polymers, polycarbazoles are known for their good electro-activity [1,2] and thermal [3][4][5], electrical [6], photo-physical [7], and electrochromic properties [8]. They have been suggested for a number of applications, such as electroluminescent devices [9], sensors [10,11], redox catalysts [12], and electrochromic displays [13]. The functional groups, such as amino, imino and sulfonic groups have been performed for achieving new polymers which meet the criteria of commercial applications [14][15][16]. There are many novel syntheses of functional polycarbazole papers. 3,6-bis (2,3-dihydrothieno [3,4-b] N-(o-ethynyl) Abstract. A novel synthesis of 4-toluene 9H-carbazole-9-carbodithioate (TCzC) was chemically synthesized and characterized by Fourier Transform Infrared (FTIR), proton nuclear magnetic resonance ( 1 H-NMR), and carbon nuclear magnetic resonance ( 13 C-NMR) spectroscopies. Specific (C sp ) and double layer capacitances (C dl ) of the electro-coated poly(carbazole) and poly(TCzC) films were obtained on glassy carbon electrode (GCE) by impedimetric method with DC potential from -0.1 to +1.0 V by increasing potential of 0.2 V. The polymers were characterized by Cyclic voltammetry (CV), Fourier transform infrared reflectance-attenuated total reflection spectroscopy (FTIR-ATR), Atomic force microscopy (AFM), and Electrochemical impedance spectroscopy (EIS). The use of additional variable (DC potential) helped to disambiguate the equivalent circuit model of R
(C(R(Q(RW))))(CR).Simulation results were compared with experimental data. In this study, substituted group effects of CS 2 and tosyl on carbazole polymer were investigated by EIS technique. CS 2 group together with tosyl group in the structure of carbazole decreased the specific capacitance value (C sp = 0.43 mF·cm -2 ) compared to PCz (C sp = 1.44 mF·cm -2 ). Electropolymerization formation was seriously affected by substituted groups of CS 2 and tosyl on conjugation system because of the electron donor and acceptor ability.