Increasing transmission of electronic interaction in dinuclear unsymmetric mixed-valent ruthenium complexes

Florencia Fagalde, Mónica E García Posse, Mónica M. Vergara, Mauricio Cattaneo, Néstor E. Katz, Isabel Romero, Teodor Parella, Antoni Llobet

Research output: Contribution to journalArticleResearchpeer-review

4 Citations (Scopus)

Abstract

The preparation and characterization by spectroscopic and electrochemical techniques of new dinuclear complexes of the type [(tpm)(bpy)RuII(L)RuII/III(NH3)5]4+/5+ (bpy = 2,2′-bipyridine), tpm = tris(1-pyrazolyl)methane, L = pz (pyrazine), 4,4′-bpy (4,4′-bipyridine), BPE (trans-1,2-bis(4-pyridyl)ethylene) and PCA (= 4-pyridinecarboxaldehyde azine), are described in this work. The analysis of the visible spectral data for the metal-to-metal charge transfer (MMCT) bands in the corresponding mixed-valent species [RubII, RuaIII] (Rub = Ru bonded to bpy; Rua = Ru bonded to NH3) allows the determination of the reorganization energies λ and electronic coupling elements HAB for the intramolecular electron transfers RubII → RuaIII mediated by L. An increased transmission of the metal-to-metal electronic interaction is disclosed for this series, when comparing the distance dependence of HAB to that of the analogous series with trpy (2,2′:6′,2″-terpyridine) acting as a spectator ligand instead of tpm. © 2006 Elsevier Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)17-23
JournalPolyhedron
Volume26
DOIs
Publication statusPublished - 2 Jan 2007

Keywords

  • Electronic interaction
  • Intervalence transitions
  • Mixed valence
  • Ruthenium dinuclear complexes
  • Scorpionate ligands

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