Ligands redox sensitive

FERROCENE AS THE CENTRAL UNIT IN NOVEL, REDOX-SENSITIVE LIGANDS, MONOMERS, AND RECEPTORS... 

Ferrocene as the central unit in novel, redox-sensitive ligands, monomers, and receptors ... 

Though thermally stable, rhodium ammines are light sensitive and irradiation of such a complex at the frequency of a ligand-field absorption band causes substitution reactions to occur (Figure 2.47) [97]. The charge-transfer transitions occur at much higher energy, so that redox reactions do not compete. 

The applications of EPR spectroscopy reviewed in the present chapter are based on the sensitivity of the spectrum displayed by iron-sulfur centers to various characteristics, such as the redox state of the center, the distribution of the valences on the iron ions, the nature and the geometry of the ligands, and the presence of nearby paramagnetic species. Although considerable progress has been made during the past few years in the quantitative analysis of these various effects in the case of the conventional iron-sulfur centers described in Section II, the discovery of centers exhibiting unusual EPR properties as... 

The structures and redox properties of these complexes have been extensively reviewed 170,171 of interest here is the presence of an intense NIR transition in the neutral and mono-anionic forms, but not the dianionic forms, i.e., the complexes are polyelectrochromic. The positions of the NIR absorptions are highly sensitive to the substituents on the dithiolene ligands. A large number of substituted dithiolene ligands has been prepared and used to prepare complexes of Ni, Pd, and Pt which show comparable electrochromic properties with absorption maxima at wavelengths up to ca. 1,400 nm and extinction coefficients up to ca. 40,000 dm3 mol-1 cm-1 (see refs. 170,171 for an extensive listing). 

As a result of their low redox potentials [173], bis(phthalocyaninato) lanthanide complexes are often inadvertently reduced or oxidized, and they are also very sensitive to acids and bases. In order to solve these problems, Veciana et al. achieved certain success on designing a series of novel compounds with characteristics that would give them improved redox stability. Electroactive ligands based on phthalo-cyaninato tetra dicarboximide [175] or perfluorinated phthalocyanine [176] were used to assemble the double-decker lanthanide complexes, with the effect of stabilizing the negative charge of the anionic state of the compounds, which resulted in a strong shift of 0.7 V of their first oxidation potentials. 

AE° = the difference between the redox potential of the complex containing the substituted ligand and that of the complex containing the unsubstituted ligand p — constant which measures the sensitivity of the redox potential to the electronic effects of the substituents a = Hammett parameter which assigns a numerical value to the electronic effects of the substituents... 

Here, p measures the sensitivity of the redox potential to substitution at a ligand L, and Eu is the sum of the Hammett, or Taft, parameters of the substituents attached to L. The symbols R, T, n, F have their usual meaning. 

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