ABSTRACT:X-Ray photoelectron spectroscopy (XPS) studies have been performed on polypyrrole-2,3-dichloro-5,6-dicyano-p-benzoquinone (PPY-DDQ) and polypyrrole-tetrachloroo-benzoquinone (PPY---chloranil) complexes prepared via the simultaneous chemical polymerization and oxidation of pyrrole by the respective acceptor. XPS data suggested that the charge transfer interactions in both complexes probably proceeded further than the pure formation of a molecular complex. The negative charges of both organic anions were mainly localized on the oxygen and the chlorine atoms and to some extent on the nitrogen of DDQ. More extensive charge transfer interaction and higher fraction of pyrrole nitrogen with positive charge were observed in the PPY-DDQ complex, which exhibited a substantially higher electrical conductivity than the corresponding PPY ---chloranil complex.KEY WORDS XPS / Polypyrrole / 2,3-Dichloro-5,6-dicyano-p-benzoquinone / Chloranil / Charge Transfer Interactions / Due to their relative physicochemical and electrical stability and well-characterized stoichiometry, highly conductive polyheterocycles, polypyrrole (PPY) in particular, have attracted a great deal of interest in recent years. 1 · 2 Most of the recent interest on conductive PPYs, however, are devoted to the materials obtained from electrochemical polymerization and oxidation. For example, most of the X-Ray photoelectron spectroscopy (XPS) studies were centered on electrochemically prepared .PPYs and related polyheterocycles.3-7 We reported recently on the XPS technique as a convenient tool for analysing the polymer-acceptor interactions in chemically synthesized PPY-halogen complexes. 8