Ligand, redox potential

Ruj1,111 11]0/ 1 11 11]- (E j2 T Interestingly, with increase of the tt-electron accepting capability in 2,2/-bipyridyl ligands, redox potentials are progressively anodic-shifted in the order 31 —> 32 —> 33 —> 34 [8]. The stabilization against... 

When the water ligands around a cation are replaced by other ligands which are more strongly attached, the redox potential can change dramatically, for example for the cobalt(II)-cobalt(III) system we have... 

Other important effects of ligand and pH changes on redox potentials will be given under the appropriate element. 

The Table shows a great spread in Kd-values even at the same location. This is due to the fact that the environmental conditions influence the partition of plutonium species between different valency states and complexes. For the different actinides, it is found that the Kd-values under otherwise identical conditions (e.g. for the uptake of plutonium on geologic materials or in organisms) decrease in the order Pu>Am>U>Np (15). Because neptunium is usually pentavalent, uranium hexavalent and americium trivalent, while plutonium in natural systems is mainly tetravalent, it is clear from the actinide homologue properties that the oxidation state of plutonium will affect the observed Kd-value. The oxidation state of plutonium depends on the redox potential (Eh-value) of the ground water and its content of oxidants or reductants. It is also found that natural ligands like C032- and fulvic acids, which complex plutonium (see next section), also influence the Kd-value. 

Similar effects are observed in the iron complexes of Eqs. (9.13) and (9.14). The charge on the negatively charged ligands dominates the redox potential, and we observe stabilization of the iron(iii) state. The complexes are high-spin in both the oxidation states. The importance of the low-spin configuration (as in our discussion of the cobalt complexes) is seen with the complex ions [Fe(CN)6] and [Fe(CN)6] (Fq. 9.15), both of which are low-spin. 

Fig. 4. Representation of the ligand sphere of the [2Fe-2S] cluster of the Rieske protein from spinach and the attribution of g-tensor to moleculEir axes as discussed in the text. Ser 130 has been observed to influence the redox potentiEd of the cluster via hydrogen interactions with the acid-labile bridging sulfur.

These share tendencies to behave as one-equivalent oxidants with redox potentials in the range 1.0 to 2.0 V and to undergo hydrolysis in aqueous solution above pH 2. They form complexes with anions, e.g. sulphate, which make their reactivity dependent on the nature of the medium both from the point of redox potential and of ligand displacement (Table 11). 

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