Fluorescence quenching rate constants, kq, ranging from 106 to 2 × 1010 M−1 sec−1, of more than 60 typical electron donor‐acceptor systems have been measured in de‐oxygenated acetonitrile and are shown to be correlated with the free enthalpy change, ΔG23, involved in the actual electron transfer process
in the encounter complex and varying between + 5 and −60 kcal/mole. The correlation which is based on the mechanism of adiabatic outer‐sphere electron transfer requires ΔG≠23, the activation free enthalpy of this process to be a monotonous function of ΔG23 and allows the calculation of rate constants of electron transfer quenching from spectroscopic and electrochemical data.
A detailed study of some systems where the calculated quenching constants differ from the experimental ones by several orders of magnitude revealed that the quenching mechanism operative in these cases was hydrogen‐atom rather than electron transfer.
The conditions under which these different mechanisms apply and their consequences are discussed.
Biomagnelism / Electron spin states / Hyperfine interaction Electron transfer processes which generate radical pairs in coherent electron spin states (singlet or triplet) are affected by weak magnetic fields [Schulten et ai, . physik. Chem. Neue Folge 101 (1976) 371]. Based on this finding we suggest a reaction mechanism for a chemical compass which exhibits a sensitivity on the orientation of the geomagnetic field originating from an anisotropy of the hyperfine interaction experienced by unpaired electron spins in a redox process. It is argued that such mechanism may explain the ability of many biological species to orient themselves in the geomagnetic field.
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