Nanosecond time-resolved absorption studies in a magnetic field ranging from zero to 3.0 T have been performed on a series of covalently linked donor-Ru(bipyridine) 3 -acceptor complexes (D-C 2+ -A 2+ ). In these complexes the electron donor is a phenothiazine moiety linked to a bipyridine by a (-CH 2 -) p (p ) 1, 4, 5, 7) chain, and the electron acceptor is an N,N′-diquaternary-2,2′-bipyridinium moiety, linked to a bipyridine by a (-CH 2 -) 2‚ chain. On the nanosecond time scale the first detectable photoinduced electron-transfer product after exciting the complex C 2+ is the charge-separated (CS) state, D + -C 2+ -A + , where an electron of the phenothiazine moiety, D, has been transferred to the diquat moiety, A 2+ . In zero field the lifetime of the CS state is about 150 ns. At low fields (B 0 < 0.5 T) the magnetic field strongly affects the decay kinetics, splitting it up into a major component, the rate constant of which decreases by a factor of about 10 at fields of several 100 mT, and a minor component with an approximately field independent rate constant. At high fields (B 0 > 0.5 T) the total amplitude of the CS absorption signal decreases and the relative contribution of the fast decaying component increases. The magnetic field effects can be consistently interpreted and quantitatively modeled by taking into account the mechanisms and kinetics of the spin multiplicity changes in the CS state and its precursor, a short-lived CT state (D-C 3+ -A + ) formed upon primary electron transfer from the triplet excited complex to the diquat moiety. Exploiting the magnetic field dependent kinetics, the rate constants of the triplet-singlet transitions in the two types of linked radical pairs and of all the electron-transfer processes following the primary one can be assessed. Magnetic-field-dependent investigations thus can be essential for the understanding of the complex kinetics in supramolecular systems with sequential cyclic electron transfer.

Page 1087, footnote 72: The value of the quantum efficiency for charge separation reported as φ cs ) 0.86 ( 0.08% is incorrect. The correct value is 86 ( 8%.

The cage escape efficiency r/ce of radicals in the electron transfer quenching of triplet methylene blue by ferrocene in acetonitrile was found to be sensitive towards an external magnetic field. The field dependence of the effect corresponding to a monotonic decrease of Bee was determined in a field range from 0.0 to 3.2 T, where it reaches a value of -20.7%. The effect is analyzed in terms of a spin chemical model wherein the effective rate of geminate reverse electron transfer, regenerating the singlet ground state of the reactants, becomes magnetic field dependent due to magnetic mixing of non-uniformly reactive spin sublevels by the anisotropic Zeeman interaction. From the analysis, the absolute values of the rate constants of spin-allowed reverse electron transfer (605 ns-~ ), cage escape (15 ns-~ ), and electron spin relaxation in the ferricenium cation (154 ns -1) could be determined.