Ferrocene poly matrix

Poly(propylene amine) dendrimers containing 4, 8, and 64 amidoferrocene peripheral units have also been incorporated in the highly ordered channels of mesoporous silica obtaining a novel type of redox-active materials. One significant feature of these new composite materials is that the ferrocene units of the guest dendrimers are easily accessible to electrochemical oxidation, as revealed by studies carried out in MeCN solutions by using Pt electrodes derivatized with films of such dendrimer-matrix complexes.33... 

Figure 5. Calibration curves for the analysis of Na and NHf ions using ion sensor made from bilayer of ferrocene-linked ormosil and dibenzo-18-crown-6 incorporated plasticized poly (vinyl chloride) matrix membrane.

Poly(ionic liquid) brushes with terminated ferrocene units acted similarly, while the interfacial resistance was probed by hexacyanoferrate [457]. Chemical and electrochemical switching of local pH at an electrode-grafted poly(vinyl pyridine) brush again allowed modulation of hexacyanoferrate chemistiy (Fig. 43) [458]. Octacyanomolybdate was used as catalyst for the oxidation of ascorbic acid [459]. Even heteropolyanions (Keggin ions) could be entrapped in polymer films electrochemicaUy [460]. Further, thermoresponsive or pH-responsive cationic copolymer films modulated the hexacyanoferrate or ferrocenedicarboxyUc acid electrochemistry by temperature or variatimi of pH and perchlorate concentration, respectively [461-463]. Besides these complexes with cationic polyelectrolyte films, electroactive cationic counterions (e.g., the europium couple) interacted with anionic networks [464]. Similarly, copper ions within a PAA matrix [367] allowed the construction of actuators [465]. Besides these binary systems (poly-electrolyte/electroactive counterions), multiresponsive electrode modification with an interpenetrating gel network of poly(acrylic) acid and poly(diethyl acrylamide) allowed the modulation of hexacyanoferrate electrochemistry [368]. 

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