Key multi(ferrocenyl) complexes in the interplay between electronic coupling and electrostatic interaction.

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.

New bis-ferrocenyl end-capped peptides: synthesis and charge transfer properties.

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.

Anti-Kasha's rule fluorescence emission in (2-ferrocenyl)indene generated by a twisted intramolecular charge-transfer (TICT) process.

A twisted intramolecular charge-transfer (TICT) process has been identified in (2-ferrocenyl)indene. This photochemical process explains the anti-Kasha's rule fluorescence emission observed for this system. Experimental and model investigations on (2-ferrocenyl)tetramethylindene and (2-ferrocenyl)-hexamethylindene were also performed, in order to evaluate the effect of a steric hindrance on the TICT mechanism. The energy of the lowest main excited states was computed with a TD-DFT approach, as a function of the rotation of the dihedral angle between the indene and the cyclopentadienyl planes. To the best of our knowledge, this is the first example of TICT generated by metal-to-ligand charge transfer (MLCT) in a ferrocene-containing complex and, more generally, the first case of complexes in which a metal center is directly involved.

Charge mapping in 3(10)-helical peptide chains by oxidation of the terminal ferrocenyl group.

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.

Metal-metal electronic coupling in syn and anti stereoisomers of mixed-valent (FeCp)2-, (RhL2)2-, and (FeCp)(RhL2)-as-indacenediide ions.

The extent of metal-metal electronic coupling was quantified for a series of syn and anti stereoisomers of (FeCp)(2)-, (RhL(2))(2)- and (FeCp)(RhL(2))- (L(2)=1,5-cyclooctadiene (cod), L=CO) as-indacenediide mixed-valent ions by spectroelectrochemical and DFT studies. The effect of the syn/anti orientation of the metal units with respect to the planar aromatic ligand indicates that electron transfer occurs through the bridge rather than through space. The nature of the metal was found to be crucial: while homobimetallic diiron species are localised valence-trapped ions (Class II), the dirhodium analogues are almost delocalised mixed-valent ions (borderline and Class III). Finally, despite their redox asymmetry, even in the heterobimetallic iron-rhodium as-indacenediide complexes, strong metal-metal coupling is present. In fact, oxidation of the iron centre is accompanied by electron transfer from rhodium to iron and formation of a reactive 17-electron rhodium site. syn and anti Fe-Rh as-indacenediide complexes are rare examples of heterobimetallic systems which can be classified as borderline Class II/Class III species.