In this review, the properties of the most significant examples of multi(ferrocenyl) cations containing a number of ferrocenyl units from two to six are discussed and the results are compared with the outcomes of some of our recent studies on conjugated ferrocenyl complexes, in order to give an overview of how the nature of the bridging ligand, the distance between the redox-active centres, and the medium affect the electronic and electrostatic properties of the molecules.

Two series of 3(10)-helical peptides of different lengths and rigidity, based on the strongly foldameric α-aminoisobutyric acid and containing a terminal ferrocenyl unit, have been synthesized. Oxidation-state sensitive spectroscopic tags of helical peptides, the N-H groups, allowed mapping of the charge delocalization triggered by oxidation of the terminal ferrocenyl moiety and were monitored by IR spectroelectrochemistry.

The foldamer field is continuously expanding as it allows to produce molecules endowed with 3D-structures and functions never observed in nature. We synthesized flat foldamers based on the natural, but non-coded, C α,β -didehydroalanine α-amino acid, and covalently linked to them two ferrocene (Fc) moieties, as redox probes. These conjugates retain the flat and extended conformation of the 2.0 5 -helix, both in solution and in the crystal state (X-ray diffraction). Cyclic voltammetry measure-ments agree with the adoption of the 2.0 5 -helix, characterized by a negligible dipole moment. Thus, elongated α-peptide stretches of this type are insulators rather than charge conductors, the latter being constituted by peptide α-helices. Also, our homo-tetrapeptide has a N-to-C length of about 18.2 Å, almost double than that (9.7 Å) of an α-helical αtetrapeptide.

Novel biferrocenyl complexes of s-and as-dihydroindacenes have been prepared and the charge transfer properties of their mono-and dicationic derivatives, selectively generated by one-electron and two-electron oxidation, have been investigated. Mixed-valence cations are generated by chemical oxidation using acetylferricinium as an oxidant agent and monitored in the visible, IR, and near-IR regions. The IT bands in the near-IR spectra are rationalized in the framework of Marcus-Hush theory. The rigid and planar indacene platform bonded to two terminal redox groups displays a redox chemistry that can be switched from single two-electron transfers to two successive one-electron transfers by changing the supporting electrolyte from nBu 4 NPF 6 to nBu 4 NB(C 6 F 5 ) 4 . § Dedicated to Prof. J€ urgen Heck on the occasion of his 60th birthday.

In this article, the successful preparation of a new series of 3(10) -helical peptides of different length containing two terminal ferrocenyl (Fc) units and based on the strongly foldameric α-aminoisobutyric (Aib) acid is reported. The synthesis of the Fc-CO-(Aib)(n) -NH-Fc (n = 1-5) homo-peptides was performed by solution methods. Moderate to good yields (26-85%) were obtained in each of the difficult coupling steps of Fc-COOH and the corresponding H-(Aib)(n)-NH-Fc compounds by C-activation with the 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide/7-aza-1-hydroxy-1,2,3-benzotriazole method. Information on the C=O···H-N intramolecularly hydrogen-bonded networks was initially obtained from FT-IR absorption measurements. The N-H stretching (amide A) region allowed us to distinguish which amide protons are involved in intramolecular hydrogen bonds and indicates the formation of an incipient 3(10) -helix structure for peptides containing at least two Aib residues. This conclusion was confirmed by (1)H NMR titrations of the N-H groups of the peptides in CDCl(3) with dimethylsulfoxide and by crystallographic analysis of the N(α) -acylated Fc-CO-(Aib)(5)-NH-Fc pentapeptide amide. The two redox-active Fc groups covalently bound to the termini of the foldameric peptide architectures were used as electrochemical probes. The end-to-end effects of electron holes generated by single and double oxidations were analyzed by means of electrochemical and spectroelectrochemical techniques. The results of these studies indicate that charge transfer across the peptide main chain does occur in the five peptides. In particular, in the pentapeptide 5, charge is transferred through an intramolecular Fe···Fe separation of 14 Å.