Polyaniline-sulfate salt

Polyaniline-sulfate salt acts as a highly efficient polymer-based solid acid catalyst in the preparation of 2-phenyl benzimidazoles and 1,5-benzodiazepines [39]. This method is applicable for the reaction of phenylenediamine with cyclic or acyclic ketones or aromatic aldehydes. The catalyst could be recycled up to six times without any loss of its activity (Scheme 17). 

U. Srinivas, C. Srirrivas, P. Narender, V.J. Rao, S. Palaniappan, Polyaniline-sulfate salt as an efficient and reusable catalyst for the s)mthesis of 1,5-benzodiazepines and 2-phenyl benzimidazoles, Catal. Commun. 8 (2007) 107-110. 

The next group of materials comprises conducting polymers (ICP). Systems with identical polymers have often been reported for polyacetylene. It is known that this ICP forms insertion compounds of the A and D types (see Section 6.4, and No. 5 in Table 12). Cells of this Idnd were successfully cycled [277, 281-283]. However, the current efficiency was only 35% heavy losses were observed due to an overoxidation of the PA [284]. In other cases as for polypyrrole (PPy), the formation of D-PPy was anticipated but did not occur [557, 558]. Entry (6) in Table 12 represents some kind of ideal model. A PPy/PPy cell with alkyl or aryl sulfates or sulfonates rather than perchlorates is claimed in [559]. Similar results were obtained with symmetric polyaniline (PANI) cells [560, 561]. Symmetric PPy and RANI cells yield about 60% current efficiency, much more than with PA. An undoped PPy/A-doped PPy combination yields an anion-concentration cell [562, 563], in analogy to graphite [47], (cf. No. 7). The same principle can be applied with the PPy/PT combination [562, 563] (cf. No. 8). Kaneto et al. [564] have reported in an early paper the combination of two pol54hiophene (PT) thin layers (< 1 pm), but the chargeability was relatively poor (Fig. 40, and No. 9 in Table 12). A pronounced improvement was due to Gottesfeld et al. [342, 343, 562, 563], who employed poly[3-(4-fluoro-phenyl)thiophene], P-3-FPT, in combination with a stable salt electrolyte (but in acetonitrile cf. Fig. 40 and No. 10 in Table 12). In all practical cases, however, Es.th was below 100 Wh/kg. 

---