Abstract
The presence of catechol during the electropolymerisation of phenylene-1,2-diamine from neutral solutions has been shown to result in a significant increase in the incorporation of phenazine redox groups into the polymer backbone. The influence of catechol concentration on the resulting redox polymer activity was investigated and a possible mechanism proposed. The versatility of the method for introducing modified phenazine groups into the polymer structure was investigated through the incorporation of two substituted catechol derivatives, 3,4-dihydroxycinnamic acid and 3,4-dihydroxybenzoic acid. The applicability of the polymer for the reduction of cytochrome c in solution was assessed by spectroelectrochemical methods. Copyright (C) 1996 Elsevier Science Ltd
| Original language | English |
|---|---|
| Pages (from-to) | 2375-2379 |
| Journal | Electrochimica Acta |
| Volume | 41 |
| Issue number | 15 |
| Publication status | Published (in print/issue) - 1996 |
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