ABSTRACT
Polyanilines (PANI) were synthesized from peroxidase-catalyzed polymerization of aniline with and without the presence of a template in the aqueous buffer solution of pH 4.3. The template used was poly(vinylphosphonic acid) (PVP). Solid-state 13C and 15N CP/MAS NMR techniques were applied to characterize the structure of polyaniline in its self-doped conducting, dedoped base, and redoped conducting form of PANI. The charge distribution along the polymer backbone in the protonated form of the polyaniline is also discussed. The structural features exhibited by a template assisted enzymatically synthesized PANI is the result of linear 1,4-coupling of aniline moiety while the PANI synthesized in the absence of template contains both 1,2- and 1,4-coupled products. Solid-state NMR studies on the enzymatically-synthesized polyaniline with the aid of template (PANI-PVP) confirmed the formation of a linear polymer chain containing alternate benzenoid-quinoid repeat units. The dedoped form is in the emeraldine base state of the polyaniline. The structural features in the spectra of the PANI synthesized without a template are quite different. Solid-state NMR data suggest that the PANI synthesized without aid of the template contains structures having C-C and C-N-C coupled products indicating the presence of branching in the polymer chain.
ACKNOWLEDGMENTS
The authors thank the National Science Foundation for the research grant (Grant # DMR-9986644). SC thanks for the summer support in part by the U.S. Army Research and Engineering Apprentice Program through the Academy of Applied Sciences, Concord, NH.
Notes
High school student for the summer of 2000 and 2001, Phillips Academy, Andover, MD.