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Hexylferrocene phosphonic acid was adsorbed on indium−tin oxide (ITO) and amino-primed ITO electrodes from ethanol. The obtained monolayers are stable in acetonitrile where cyclic voltammetry shows the formation of domains of self-interacting and free ferrocene molecules. Distinct phases are observed on bare ITO, whereas a single Frumkin isotherm is obtained on amino-primed ITO. Dilution experiments with alkylphosphonic acids C n H 2 n +1 PO(OH) 2 ( n = 3, 6, and 12) have shown that only the dodecyl chain may compete with the hexylferrocene chain, which remains 50 times more strongly bound to the surface. The free energy of self-interaction of the ferrocene moieties in the layers is ca. 40 kJ mol - 1; that is, it is equivalent to that of a 15 carbon atom alkyl chain. Lateral interactions among hexylferrocene and dodecyl chains form isolated domains of the components, ruling out a real dilution of ferrocenes to single isolated molecules.
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Vercelli et al. (2003) studied this question.
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