In this report, two new redox-responsive complexes with different dendritic tail chain number (P4VP- nFc, n = 1, 2) were prepared via the hydrogen-bonded self-assembly of poly(4-vinylpyridine) and ferrocenyl-modified percec-type… Click to show full abstract
In this report, two new redox-responsive complexes with different dendritic tail chain number (P4VP- nFc, n = 1, 2) were prepared via the hydrogen-bonded self-assembly of poly(4-vinylpyridine) and ferrocenyl-modified percec-type dendrons. These complexes exhibited a crystalline phase for P4VP-1Fc and liquid crystalline for P4VP-2Fc at room temperature. The cyclic voltammetry measurement shows that the electrode process of P4VP-nFc (n = 1, 2) films was diffusion controlled and the reversibility of the electrode process for the P4VP-2Fc films became better than that for the P4VP-1Fc. Moreover, the redox peak current |ip| increased with increasing dendritic tail chain number n in the complex, because the complex film formed with 2Fc-COOH has the looser stacking of alkyl chains, which was favorable for the electrolyte diffusion and charge transfer. The present results demonstrate that the electrochemical activity of the redox-responsive poly(4-vinylpyridine) -ferrocenyl dendron complex can be easily tuned using the dendritic tail chain with different numbers. These complexes may be used as new kinds of modified electrodes.
               
Click one of the above tabs to view related content.