A divinylphenylene bridged diruthenium complex constitutes an ensemble of three coupled redox systems. Spectroelectrochemistry provides evidence that the oxidation processes are dominated by the organic bridge.

Reversible redox-switching of through-bond magnetic interaction has been achieved by conformation change of the tetraarylethylene moiety upon redox input: intramolecular magnetic interaction between two nitroxide groups is dead after oxidation, whereas it was alive before.

Using a purification method introduced earlier based on redox properties it was possible to isolate Sc3N@I(h)-C80 and Sc3N@D(3h)-C78 and a mixture of Sc3N@D(5h)-C80 and Sc3N@D3-C68. Taking advantage of their chemical reactivity differences, Sc3N@D(5h)-C80 was isolated from Sc3N@D3-C68 followed by further functionalization, giving rise to five new methano-derivatives of Sc3N@D(5h)-C80.

A diagram of energies between the HOMO of donor (D) and LUMO of acceptor (A) vs.ΔE(1/2)(DA) (= E(1/2)(D) - E(1/2)(A): E(1/2) = first-redox potential) clearly demonstrates the ionicity in the series of D/A assemblies, [{Ru(2)(CF(3)CO(2))(4)}(2)(TCNQR(x))]·n(solv) (TCNQR(x) = 2,5- or 2,3,5,6-R-substituted 7,7,8,8-tetracyano-p-quinodimethane; R(x) = H(4), F(2), Cl(2), Br(2), F(4), Me(2), (OMe)(2)).

The first synthesis of the two-electron reduction product of a pyrylogen is reported. The magnitude of the experimentally determined disproportionation constant for a pyrylogen radical cation was used to advantage in order to provide compelling evidence for formation of this reduction product. Computational studies were used to provide verification of these results and to provide additional ins...

Described here is a semiquantitative theoretical treatment of the kinetics of outer sphere electrochemical reactions. The framework presented here, which is based on simple physical arguments, predicts heterogeneous rate constants consistent with previous experimental observations (k0 > 10 cm/s). This theory is applied to the analysis of voltammetry experiments involving ultramicroelectrodes mo...

Metallamacrocylic tetraruthenium complexes were generated by treatment of 1,4-divinylphenylene-bridged diruthenium complexes with functionalized 1,3-benzene dicarboxylic acids and characterized by HR ESI-MS and multinuclear NMR spectroscopy. Every divinylphenylene diruthenium subunit is oxidized in two consecutive one-electron steps with half-wave potential splittings in the range of 250 to 330...

First-row two-coordinate complexes are attracting much interest. Herein, we report the high-yield isolation of the linear two-coordinate iron(I) complex salt [K(L)][Fe{N(SiMe3 )2 }2 ] (L=18-crown-6 or crypt-222) through the reduction of either [Fe{N(SiMe3 )2 }2 ] or its three-coordinate phosphine adduct [Fe{N(SiMe3 )2 }2 (PCy3 )]. Detailed characterization is gained through X-ray diffraction, v...

We reconsider the Nagelian theory of reduction and argue that, contrary to a widely held view, it is the right analysis of intertheoretic reduction. The alleged difficulties of the theory either vanish upon closer inspection or turn out to be substantive philosophical questions rather than knock-down arguments.