Molecular mixed-valence cyanide bridged Co-III-Fe-II complexes


Autoria(s): Bernhardt, P. V.; Bozoglian, F.; Macpherson, B. P.; Martinez, M.
Data(s)

01/01/2005

Resumo

Cyano-bridged mixed-valence compounds have been known for a long time, i.e., Prussian Blue polymeric solids. Nevertheless, the interest in discrete complexes having a well-defined molecular nuclearity has emerged more recently. There are numerous examples of cyano-bridged mixed-valence complexes in the recent literature, as they show promising and useful applications in electrochromism, molecular magnetism and molecular electronics. In this paper, the reactivity, synthetic and structural chemistry, as well as some physical and chemical properties, of a series of discrete dinuclear mixed-valence cyano-bridged complexes of general formulae [LnCoIII(mu NC)Fe-II(CN)(5)](-) (L = pentadentate macrocyclic ligand) are reviewed. Special emphasis is given to the synthetic strategy, redox properties and metal-to-metal-charge-transfer (MMCT) band energy. Tuning the MMCT transition energy has been possible by changing the redox potential of the metal centers, both through structural and outer-sphere changes. The redox processes that involve the appearance and disappearance of these MMCT bands in the visible region have been dealt with in relation to the possible uses of the complexes. (c) 2004 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:75617

Idioma(s)

eng

Publicador

Elsevier Science Sa

Palavras-Chave #Mixed-valence Compounds #Metal-to-metal-charge-transfer Band Energy #Outer-sphere Oxidation #Chemistry, Inorganic & Nuclear #Sphere Redox Reactions #Electron-transfer Reactions #Transfer Absorption-band #Intervalence Transfer #Substitution-reactions #Cobalt(iii) Complexes #Photoredox Reactions #Ferricyanide Ion #Aqueous-solution #Metal-complexes #C1 #250201 Transition Metal Chemistry #780103 Chemical sciences
Tipo

Journal Article