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Updated: May 23, 2026

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Efficient energy transfer via the cyanide bridge in dinuclear complexes containing Ru(II) polypyridine moieties
Alejandro Cadranel1, Pablo Alborés, Shiori Yamazaki
1Departamento de Química Inorgánica, Analítica y Química Física, INQUIMAE, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón 2, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina.
Abstract:
We report the synthesis, structure and properties of the cyanide-bridged dinuclear complex ions [Ru(L)(bpy)(μ-NC)M(CN)(5)](2-/-) (L = tpy, 2,2';6',2''-terpyridine, or tpm, tris(1-pyrazolyl)methane, bpy = 2,2'-bipyridine, M = Fe(II), Fe(III), Cr(III)) and the related monomers [Ru(L)(bpy)X](2+) (X = CN(-) and NCS(-)). All the monomeric compounds are weak MLCT emitters (λ = 650-715 nm, ϕ ≈ 10(-4)). In the Fe(II) and Cr(III) dinuclear systems, the cyanide bridge promotes efficient energy transfer between the Ru-centered MLCT state and a Fe(II)- or Cr(III)-centered d-d state, which results either in a complete quenching of luminescence or in a narrow red emission (λ ≈ 820 nm, ϕ ≈ 10(-3)) respectively. In the case of Fe(III) dinuclear systems, an electron transfer quenching process is also likely to occur.
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