Electrolyte effects on the intervalence transition within discrete binuclear cyano-bridged complexes. An estimation of activation free energy from static, optical and electrochemical data |
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Authors: | P. Pé rez-Tejeda,G. Ló pez-Pé rez,F. Sá nchez,M. Ló pez-Ló pez,G. Gonzá lez |
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Affiliation: | a Departamento de Química Física, Facultad de Química, Universidad de Sevilla, c/Prof. García González s/n, 41012 Sevilla, Spain b Departament de Química Inorgànica, Universitat de Barcelona, Martí i Franquès 1-11, E-08028 Barcelona, Spain |
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Abstract: | A study of the metal-to-metal charge-transfer (MMCT) transition within the binuclear cyano-bridged complexes cis-[L13CoIII(μ-NC)FeII(CN)5]− (L13 = 12-methyl-1,4,7,10-tetraazacyclotridecan-12-amine), trans-[L14CoIII(μ-NC)FeII(CN)5]− (L14 = 6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine) and trans-[L15CoIII(μ-NC)FeII(CN)5]− (L15 = 10-methyl-1,4,8,12-tetraazacyclopentadecan-10-amine) has been carried out in electrolyte solutions at varying concentrations. Using these data, as well as the reaction free energies obtained from electrochemical measurements, the reorganisation and activation free energies for the forward and reverse thermal electron-transfer processes have been estimated. The changes of these parameters with the electrolyte concentration, as well as those of the energy of the maximum MMCT band and the reaction free energy, are mainly due to ion-pairing effects. |
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Keywords: | Marcus-Hush Ion-pairing Cyano-bridged complexes Static data |
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