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Mixed-valency with cyanides as terminal ligands: Diruthenium(III,II) complexes with the 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine bridge and variable co-ligands (CN- vs. bpy or NH3)

  1. 1.
    SYSNO ASEP0341711
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMixed-valency with cyanides as terminal ligands: Diruthenium(III,II) complexes with the 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine bridge and variable co-ligands (CN- vs. bpy or NH3)
    Author(s) Vergara, M. M. (AR)
    García Posse, M. E. (AR)
    Fagalde, F. (AR)
    Katz, N. E. (AR)
    Fiedler, Jan (UFCH-W) RID, ORCID
    Sarkar, B. (DE)
    Sieger, M. (DE)
    Kaim, W. (DE)
    Source TitleInorganica chimica acta. - : Elsevier - ISSN 0020-1693
    Roč. 363, č. 1 (2010), s. 163-167
    Number of pages5 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordscyano ligands ; mixed-valency ; Ruthenium complexes
    Subject RIVCG - Electrochemistry
    R&D ProjectsOC 140 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    OC09043 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000272205800021
    DOI10.1016/j.ica.2009.09.018
    AnnotationNew diruthenium complexes (PPN)(4)[(NC)(4)Ru(mu-bptz)Ru(CN)(4)], (PPN)(4) 1, and [(bpy)(2)Ru(mu-bptz)Ru(CN)(4)], 2, (PPN+ = bis(triphenylphospine)iminium; bptz = 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine; bpy = 2,2'-bipyridine), were synthesised and characterised by spectroscopic and electrochemical techniques. The comproportionation constant K-c = 10(7.0) of the mixed-valent species [(NC)(4)Ru(mu-bptz)Ru(CN)(4)](3) as obtained by oxidation of 1(4) in CH3CN is much lower than the K-c = 10(15.0) previously detected for [(H3N)(4)Ru(bptz)-Ru(NH3)(4)](5+), reflecting the competition between CN and bptz for the p-electron density of the metals. Comparison with several other bptz-bridged diruthenium(II, III)complexes reveals an approximate correlation between K-c and the diminishing effective pi acceptor capacity of the ancillary terminal ligands.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2011
Number of the records: 1  

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