It was recently reported that water soluble conducting polyaniline may be p
repared using a new template-guided enzymatic approach. To address the mech
anistic role of the template in this reaction, various macromolecular and s
urfactant templates were investigated. It was found that the template provi
des a necessary type of "local" environment where the pH and charge density
near the template molecule is different from that of the bulk solution. C-
13 and H-1 NMR studies showed that this "local" environment serves as a typ
e of nano-reactor that is critical in anchoring, aligning, and reacting the
aniline monomers and ultimately controls what form of polyaniline (conduct
ing or insulating) is obtained during reaction. Strong acid polyelectrolyte
s, such as sulfonated polystyrene (SPS), are the most favorable because the
y provide a lower, local pH environment that serves to both charge and pref
erentially align the aniline monomers through electrostatic and hydrophobic
interactions to promote the desired head-to-tail coupling. Interestingly,
it was found that micelles formed from aggregating, strong acid surfactant
molecules such as sodium dodecylbenzenesulfonic acid (SDBS) also provide su
itable local template environments that lead to the formation of conducting
polyaniline. H-1 NMR spectral data showed that the aniline monomers in the
se micelle systems intercalate between the sulfonated styrene headgroups of
the micelles. However, if the reaction media was such that micelles were n
ot formed or if the distance between the sulfonated headgroups in the mixed
micelle systems was too large, then the conducting form of polyaniline cou
ld not be obtained. The information gained from this study strongly support
s the existence and importance of "local" template environments in guiding
the enzymatic synthesis of polyaniline. A fundamental understanding of thes
e types of mechanisms should lead to the design and optimization of a broad
range of other interesting template-guided reactions.