Number of the records: 1  

Synthesis and electrochemical study of iron, chromium and tungsten aminocarbenes Role of ligand structure and central metal nature

  1. 1.
    SYSNO ASEP0357153
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSynthesis and electrochemical study of iron, chromium and tungsten aminocarbenes Role of ligand structure and central metal nature
    Author(s) Hoskovcová, I. (CZ)
    Roháčová, J. (CZ)
    Dvořák, D. (CZ)
    Tobrman, T. (CZ)
    Záliš, Stanislav (UFCH-W) RID, ORCID
    Zvěřinová, R. (CZ)
    Ludvík, Jiří (UFCH-W) RID, ORCID
    Source TitleElectrochimica acta. - : Elsevier - ISSN 0013-4686
    Roč. 55, č. 27 (2010), s. 8341-8351
    Number of pages11 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsFischer aminocarbene complexes ; Voltammetry-polarography ; HOMO-LUMO displacement
    Subject RIVCG - Electrochemistry
    R&D ProjectsIAA400400813 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000284434700081
    DOI10.1016/j.electacta.2010.02.057
    AnnotationSeveral series of Fischer-type aminocarbene complexes with central Fe Cr or W atoms and with various carbene substitution were synthesized and electrochemically investigated by dc-polarography and cyclic voltammetry. The shifts and changes of reduction and oxidation potentials were evaluated using the linear free energy relationship (LFER) approach with respect to (a) the type of coordination (b) the substitution on the carbene ligand and (c) the nature of the central metal atom. The analysis of measured data confirms that the reduction center is localized on the carbene moiety and is strongly influenced by both electronic and sterical properties of its substituents. The oxidation proceeds on the metal and depends mainly on its nature and on the pi-acidity of the ligands. Electrochemistry thus represents an important experimental approach to the description and understanding of the molecular electronic structure and redox properties.
    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  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.