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It is demonstrated that polyaniline can be solubilized in nitromethane via complexation with SnCl 4 . The solutions of PANI−SnCl 4 complex show UV−vis−NIR spectral features distinctly different from those reported for Brönsted acid doped PANI. The removal of the solvent results in the formation of a free-standing film of SnCl 4 -doped PANI. The solid-state complex shows the stoichiometry of PANI(SnCl 4 ) 1.0 (CH 3 NO 2 ) 1.0, which means that both types of polyaniline nitrogens (imine and amine) participate in the complexation reaction and one solvent molecule is introduced in the polymer matrix per one Lewis acid molecule. Mössbauer parameters of the complex (IS = 0.43 mm/s vs SnO 2, QS = 0.49 mm/s) are consistent with hexacoordinated Sn(IV) in an environment of nonequivalent ligands. XPS studies are in good agreement with Mössbauer spectroscopy, giving Sn3d XP spectra characteristic of SnCl 4 ·2L complexes. Similar complexation can be achieved in dried PANI(HCl) 0.5; however, in this case, SnCl 4 is complexed only on nonprotonated nitrogen sites.
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Kulszewicz‐Bajer et al. (1999) studied this question.
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