Abstract
The immobilization of dinuclear copper(II) acetate complexes (Cu2(CH3COO)4·2H2O) on self-assembled monolayers (SAMs) of different aliphatic and aromatic thiols with oxygen and nitrogen donors at the end group is investigated on preferentially oriented (111) gold surfaces (Au(111)). The Cu species are immobilized at the outer plane of these terminal groups by the interaction of the terminal moiety of the functionalized SAMs. The highest electrochemical activity for the Cu(II)/Cu(I) redox couple is found for the metallic complexes immobilized on SAMs of short thiols, irrespective of their aliphatic or aromatic character, or the nature of the terminal group of the linking molecule, suggesting that direct tunneling is the main path for charge transfer to the Au substrate. Even though a progressive demetalation of the copper acetate complex immobilized on N-terminated SAMs by the release of Cu ions to the solution is induced by repeated potential scans, this process is negligible for Cu species immobilized on ...
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